Skip to main content

Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort



In North African populations, G2019S mutation in LRRK2 gene, encoding for the leucine-rich repeat kinase 2, is the most prevalent mutation linked to familial and sporadic Parkinson’s disease (PD). Early detection of G2019S by fast genetic testing is very important to guide PD’s diagnosis and support patients and their family caregivers for better management of their life according to disease’s evolution.


In our study, a genetic PD’s diagnosis tool was developed for large scale genotyping using Kompetitive Allele Specific PCR (KASP) technology. We investigated G2019S’s frequency in 250 Tunisian PD patients and 218 controls.


We found that 33.6% of patients and 1.3% of controls were carriers. Demographic characteristics of patients with G2019S had no differences compared with non-carrier patients. Thereby, we could emphasize the implication of G2019S in PD without any distinctive demographic factors in the studied cohort. Sixty patients out of 250 were genotyped using Taqman assay and Sanger sequencing. The genotyping results were found to be concordant with KASP assay.


The G2019S mutation frequency in our cohort was similar to that reported in previous studies. Comparing to Taqman assay and Sanger sequencing, KASP was shown to be a reliable, time and cost effective genotyping assay for routine G2019S screening in genetic testing laboratories.

Peer Review reports


In the last decade, genetic research has made tremendous progress in identifying the genetic etiology of Parkinson’s disease (PD). Mutations in LRRK2 gene, encoding for the leucine-rich repeat kinase 2, were found to be the most frequent cause of late-onset autosomal dominant form of PD [1, 2]. The LRRK2 gene, located on chromosome 12q12 with 51 exons, encodes a highly conserved 2527 amino-acid multi-domain protein having kinase and GTPase functions [3]. Among 80 missense variants in LRRK2 gene, 7 mutations are associated with dominantly inherited forms of PD, and are clustered in functionally important regions [4]. The most prevalent LRRK2 mutation is the c.6055 G > A in exon 41, which causes a glycine to serine substitution (G2019S) in the highly conserved activation loop of its MAP kinase domain [5]. The G2019S was shown to have a worldwide distribution [6]. Globally, this mutation occurs in 3 to 6% of familial PD and in 1 to 2% of sporadic PD [7]. However, its frequency varied greatly according to geographical or ethnic origin with the highest values seen in North African (37% of familial PD and 41% of sporadic PD) and Ashkenazi Jews (30% of familial PD and 13% of sporadic PD). Lower frequencies of this mutation were observed in sporadic and familial PD patients in North American (3 and 1%), European (4 and 1%) and Asian populations (0.1 and 0%) [6].

Although it is rarely found in healthy controls, genetic testing for LRRK2 mutations is very important to support PD patients and their families. Thus, a fast and accurate genotyping method should be taken into account to screen the G2019S mutation. Early genotyping routine was commonly based on direct sequencing. This technique was then replaced by real-time polymerase chain reaction (PCR) based genotyping methods including TaqMan assay and high resolution melting technique. These methods are low-priced, less time-consuming and highly-sensitive. Recently, the Kompetitive Allele Specific PCR (KASP) genotyping assay has been successfully used to validate DNA polymorphisms. This uniplex, fluorescence-based genotyping technology, is based on allele-specific primer extension [8]. It offers the simplest and the most cost-effective way to determine precisely single-nucleotide polymorphism (SNP) genotypes.

In this work, we used KASP genotyping assay to screen the LRRK2 G2019S mutation in a cohort of Tunisian PD patients. Through this technique, we aimed to develop a genetic diagnostic tool for large scale genotyping.


Patients and control subjects

A series of 250 Tunisian unrelated PD patients (96 familial and 154 apparently sporadic cases) were recruited at the Neurology Department, Razi Hospital (La Manouba, Tunisia). Patients were diagnosed as being affected if they satisfied the United Kingdom Parkinson’s disease Society (UKPDS) brain bank criteria, except the exclusion of family history of PD. In addition to PD patients, 218 Tunisian unrelated control subjects were recruited from different primary care clinics. They did not have symptoms or family history of neurological disorders.

KASP genotyping assay

Genomic DNA was extracted from peripheral blood of subjects using the Salting-out method [9]. The 468 DNA samples, including 250 PD patients and 218 controls, were genotyped using the KASP assay.

The KASP assay mix required to determine SNP genotypes was purchased from LGC Genomics (Beverly, MA) using ‘KASP by Design’ method. The SNP of interest (rs34637584) and a 500 base-pairs (bp) sequence surrounding the SNP were annotated with known variants using ENSEMBL genome browser and were submitted to LGC Genomics website via their SNP submission template. The designed KASP assay mix comprised three primers (two allele-specific and one common reverse primer).

DNA samples were dispatched in 96-well plates. Two DNA controls were included in each reaction plate. The DNA controls were samples from one normal individual and a second individual heterozygous for the G2019S mutation selected from Whole Exome Sequencing (WES) data collected from the database of the Laboratory of Biomedical Genomics and Oncogenetics. No positive homozygous control was available. KASP reactions were done following the manufacturer’s protocol (LGC Genomics, Beverly, MA) using 50 ng of DNA in a 5 μl reaction volume. Reactions were carried-out in a 96-Well Light Cycler 480 II (Roche, CA) at the following conditions: 94 °C for 15 min, then 10 cycles of 94 °C for 20 s, 61 °C for 1 min, followed by 26 cycles of 94 °C for 20 s and 1 min at 55 °C. Following the PCR, fluorescence was detected using a single quantification cycle of 37 °C for 1 s after cooling at 37 °C for 1 min. Data were analyzed using the “Endpoint Genotyping” method of the Light Cycler 480 Software (release 1.5.0).

TaqMan assay

Among the 250 PD patients, 60 were screened for LRRK2 G2019S mutation by an allelic discrimination Taqman assay. According to the manufacture’s manual, the genotyping reaction was composed of TaqMan universal PCR master mix (Applied Biosystems Master Mix, catalogue number 4351379), TaqMan SNP genotyping reagent which included forward and reverse primers and SNP specific probe labeled with VIC dye conjugated to the 5′ end of the wild type allele probes and FAM dye conjugated to the 5′ end of the mutated allele probes. Allelic discrimination was automatically carried-out with PRISM 7000 sequence detection system (Applied Biosystems, CA).

Sanger sequencing

Exon 41 of LRRK2 gene was amplified by PCR from genomic DNA of 60 PD patients (already genotyped by Taqman and KASP assay) using two primers: 5′-TTTCCTGTGCATTTTCTGGCA-3′ and 5′-TGAGACAGACCTGATCACCTA-3′ under the following reaction conditions: denaturation at 95 °C for 5 min followed by 30 cycles of 95 °C for 30 s, 60 °C for 30 s and 72 °C for 30 s; and a final cycle of 7-min extension at 72 °C. PCR products were purified and sequenced using the Big-dye terminator Cycle Sequencing Kit v1.1 on an 3500xL Genetic Analyzer DNA sequencer (Applied Biosystems, CA). Sequences were analyzed using the Seqscape software (Applied Biosystems, CA).

Statistical analyses

Statistical analyses were conducted using GraphPad Prism software version 5.03. The rs34637584 genotypes were examined for deviation from Hardy-Weinberg equilibrium (HWE) using Chi-square test. Statistical comparison of PD patients and controls with and without the G2019S mutation was performed where appropriate using Fisher’s exact test and F-test to compare variance.


Tunisian PD patients (250) and controls (218) were genotyped using the KASP assay. Our study revealed that the LRRK2 G2019S mutation was present in 84 of 250 PD patients (33.6%) and in 3 of 218 controls (1.3%). Among the eighty-four G2019S carriers, 76 were heterozygous (30.4%) and 8 were homozygous (3.2%) for the mutation. No deviation from HWE was observed among PD patients (P > 0.05). All control G2019S carriers (3 individuals) were heterozygous. The frequency of the mutation among patients with familial cases (96 patients) was 37.5% (36 patients, 30 heterozygous and 6 homozygous) and 31% (48 patients, 46 heterozygous and 2 homozygous) in sporadic cases (154 patients).

In order to assess the accuracy of the KASP assay, genotyping results of 60 DNA samples of PD patients were verified through TaqMan assay and Sanger sequencing. Genotyping results were identical to those obtained by KASP.

Demographic characteristics of PD patients and controls were shown in Table 1. Both groups have equivalent sex ratios and similar mean age and age of onset. Demographic data of patients were stratified according to LRRK2 G2019S (Table 2). The means of age of onset and gender distribution were not significantly different between carriers (homozygous and heterozygous individuals) and non-carriers. Furthermore, it seemed that the presence of G2019S mutation did not have an effect on the clinical picture of the sporadic nor on the familial form of PD. The mean age of onset was relatively similar in carriers (56.4 ± 13 for sporadic vs 55.8 ± 12.4 for familial, p = 0.76) and non-carriers (61.8 ± 10.8 for sporadic vs 55.8 ± 12.9 for familial, p = 0.12).

Table 1 Demographics of Patients and Control subjects
Table 2 Demographics of PD patients with and without LRRK2 G2019S mutations


In the present study, we reported a large series of Tunisian patients in which the high frequency of the G2019S mutation seemed to be the cause of autosomal dominant PD. The mutation frequency among patients (33.6% of total, 37.5% of familial cases and 31% for sporadic cases) was in agreement with previously reported series of PD patients from Tunisia and North Africa. Frequency studies revealed a strikingly high value in North Africa (40.3% of familial and 33% of sporadic cases) [6]. Therefore, the G2019S mutation could be considered of clinical utility for the early molecular diagnosis and treatment of PD.

The mutation was also present in a 1.3% of control individuals. According to published reports, one of the highest frequencies of G2019S was found in North African controls (1.5%) [6]. Moreover, genetic screening in North African unrelated healthy subjects showed that the incidence of G2019S was 1.57% in 127 Tunisian controls [10]. However, the mean age of controls with G2019S mutation was lower than the general mean age at onset of PD. These individuals might be considered at risk carriers that could eventually develop PD within a decade or could probably be in the prodromal phase of PD.

Previous studies reported Tunisian families included in large cohorts of heterogeneous ethnic groups and G2019S frequencies were calculated for the whole North African population including Tunisia, Algeria and Morocco [7, 11, 12]. Specific data concerning the G2019S mutation in the Tunisian population were included only in three different reports summarized in Table 3. We noted that there was no overlap between our cohort and those described in previous studies. The first study reported a frequency of 42% in 91 Tunisian families [13] and a common ancestral founding haplotype was shared by these families and those from the United States, as well as from several European and Middle Eastern countries [14]. The second report was a case-control study performed on 238 patients with sporadic PD and 371 controls [15]. Later, clinical features of LRRK2 G2019S parkinsonism were studied in a 570 unrelated and 288 related patients including 220 sporadic (38%) and 126 familial cases (45%) who were carriers of the mutation [16]. In the same report, the mutation was also detected in 12 of 580 unrelated controls (3%).

Table 3 Summary of previous screening studies of the G2019S mutation in the Tunisian population

In our study, the age of onset was similar between LRRK2 G2019S homozygous, heterozygous and non-carriers. Moreover, in these three groups, no significant differences of age of onset were shown when familial and sporadic forms were compared. These results were in accordance with previous Tunisian cohort studies [15, 16]. However, Ishihara et al. [13] reported that both homozygous and heterozygous G2019S individuals were older at onset than non-carrier patients. This difference could be explained by the familial nature of the study, including only related individuals (Table 3). In future studies, the screening strategy of the LRRK2 G2019S mutation in the Tunisian population would focus on the recruitment of symptomatic individuals, regardless of age, gender or family history.

Through the development of whole genome sequencing by next-generation sequencing (NGS) technologies, a large number of polymorphic SNP linked to neurodegenerative disease were identified. The classic genotyping method using Sanger sequencing and PCR-RFLP were costly and labor-intense. Thus, a high-throughput and cost effective platform was required to carry out large-scale genotyping of these SNPs of interest.

The KASP genotyping system has been used widely and successfully over many years in the field of genetic improvement of animals and field crops [8]. In our work, we screened the rs34637584 in 250 PD patients using KASP genotyping assay. Sixty samples out of 250 were then screened by Taqman and Sanger sequencing in order to assess the reliability and the cost of methods used.

Unlike Sanger sequencing, both KASP and Taqman assays possessed mutual advantages, like low-labor, cost and high-tolerance of variability in DNA quantity and quality. The assays could be conducted for large numbers of samples within a short period of time without post-PCR handling [8, 17]. These properties are critical for a large-scale genetic testing. Moreover, KASP and Taqman genotyping PCR’s are suitable for use on a variety of real-time PCR instruments. However, the main drawback for these assays is their limited capacity to be used for SNP multiplexing.

Furthermore, KASP had higher advantage than Taqman. It did not require labelling of the SNP-specific primers which reduced the cost. Thus, KASP genotyping offered by different laboratory worldwide showed a significant cost saving option compared to common Taqman technologies. According to previous studies and some commercial genotyping service providers, the current KASP reaction costs five times cheaper than Taqman. Moreover, a study of SNP selection for the soybean genotyping [17] has shown that allele-specific assay cost 0.005 US$ for KASP compared to 0.238 US$ for Taqman.

In addition, KASP allows a greater flexibility for primer design which increased overall success rate and offerd an exceptionally accurate genotyping solution. Previous work has assessed the effectiveness of KASP genotyping technologies compared to Taqman or Sanger sequencing. According to an application note published by the University of Nottingham, the KASP technique was more efficient than TaqMan in terms of successful design of custom genotyping assays for a rare variant associated with Alzheimer’s disease [18].

The LRRK2 G2019S mutation was screened in populations worldwide using classical targeted sequencing, High-resolution melting analysis and TaqMan genotyping assay. Ours was the first study using KASP genotyping to screen this recurrent mutation. KASP was used to genotype other SNP’s linked to PD, like the LRRK2 variant rs1491942 and other SNPs in the PARK16 locus in a Scandinavian population [19]. Besides, this technique was used to screen for variants in regulatory regions of SNCA associated with PD [20]. It was often required to confirm the association of rare variants with a particular phenotype like the rare R1205H and D620N mutations of 4G1 and VSP gene, respectively, in South African PD patients [21]. Moreover, KASP genotyping assay was recently used to screen SNPs in different neurological disorder like Alzheimer’s disease (rs75932628 of TREM2 [22], rs1476679 of ZCWPW1 gene [23] and both rs7412 and rs429358 for Apolipoprotein E genotyping [24]), amyotrophic lateral sclerosis [25], genetic generalized epilepsy (VRK2 rs2947349 [26]) and polyglutamine diseases [27].


By using KASP genotyping assay, we have shown that the G2019S mutation frequency in a PD Tunisian patient’s cohort was similar to that reported in previous studies. The KASP technique could be a reliable genotyping assay for routine mutation screening in genetic testing. The implementation of this diagnostic activity within hospitals in Tunisia and in other North African or emerging countries will pave the way for personalized medicine in these countries and could improve the management of PD patients and their families.



Hardy-Weinberg equilibrium


Kompetitive Allele Specific PCR


Leucine-rich repeat kinase 2


Polymerase chain reaction


Parkinson’s disease


Single-nucleotide polymorphism


United Kingdom Parkinson’s disease Society


Whole exome sequencing


  1. Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, van der Brug M, Lopez de Munain A, Aparicio S, Gil AM, Khan N, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson’s disease. Neuron. 2004;44(4):595–600.

    Article  CAS  PubMed  Google Scholar 

  2. Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron. 2004;44(4):601–7.

    Article  CAS  PubMed  Google Scholar 

  3. Cookson MR. Cellular effects of LRRK2 mutations. Biochem Soc Trans. 2012;40(5):1070–3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Rudenko IN, Cookson MR. Heterogeneity of leucine-rich repeat kinase 2 mutations: genetics, mechanisms and therapeutic implications. Neurotherapeutics. 2014;11(4):738–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Mata IF, Wedemeyer WJ, Farrer MJ, Taylor JP, Gallo KA. LRRK2 in Parkinson's disease: protein domains and functional insights. Trends Neurosci. 2006;29(5):286–93.

    Article  CAS  PubMed  Google Scholar 

  6. Correia Guedes L, Ferreira JJ, Rosa MM, Coelho M, Bonifati V, Sampaio C. Worldwide frequency of G2019S LRRK2 mutation in Parkinson’s disease: a systematic review. Parkinsonism Relat Disord. 2010;16(4):237–42.

    Article  CAS  PubMed  Google Scholar 

  7. Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Durr A, Brice A. LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet. 2005;77(2):330–2.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. He C, Holme J, Anthony J. SNP genotyping: the KASP assay. Methods Mol Biology (Clifton, NJ). 2014;1145:75–86.

    Article  CAS  Google Scholar 

  9. Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Change N, Mercier G, Lucotte G. Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects. Genet Test. 2008;12(3):333–9.

    Article  CAS  PubMed  Google Scholar 

  11. Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, et al. Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson’s disease patients from 18 countries. Mov Disord. 2006;21(8):1102–8.

    Article  PubMed  Google Scholar 

  12. Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, Leutenegger AL, Guimaraes J, Bonnet AM, Agid Y, et al. G2019S LRRK2 mutation in French and North African families with Parkinson’s disease. Ann Neurol. 2005;58(5):784–7.

    Article  CAS  PubMed  Google Scholar 

  13. Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari PA, et al. Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson’s disease families. Mov Disord. 2007;22(1):55–61.

    Article  PubMed  Google Scholar 

  14. Warren L, Gibson R, Ishihara L, Elango R, Xue Z, Akkari A, Ragone L, Pahwa R, Jankovic J, Nance M, et al. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson’s disease. Parkinsonism Relat Disord. 2008;14(1):77–80.

    Article  CAS  PubMed  Google Scholar 

  15. Hulihan MM, Ishihara-Paul L, Kachergus J, Warren L, Amouri R, Elango R, Prinjha RK, Upmanyu R, Kefi M, Zouari M, et al. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Lancet Neurol. 2008;7(7):591–4.

    Article  CAS  PubMed  Google Scholar 

  16. Trinh J, Amouri R, Duda JE, Morley JF, Read M, Donald A, Vilarino-Guell C, Thompson C, Szu Tu C, Gustavsson EK, et al. Comparative study of Parkinson’s disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism. Neurobiol Aging. 2014;35(5):1125–31.

    Article  CAS  PubMed  Google Scholar 

  17. Yuan J, Wen Z, Gu C, Wang D. Introduction of high throughput and cost effective SNP genotyping platforms in soybean. Plant Genet Genomics Biotechnol. 2014;1(3):90–4.

    Article  Google Scholar 

  18. Braae A, Thompson C, Morgan K: Comparison of custom designed KASP and TaqMan genotyping assays for a rare genetic variant identifed through resequencing GWAS loci. LGC, University of Nottingham - app note:2014.

  19. Pihlstrom L, Rengmark A, Bjornara KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, et al. Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease. J Hum Genet. 2015;60(7):357–62.

    Article  PubMed  Google Scholar 

  20. Schmitt I, Wullner U, van Rooyen JP, Khazneh H, Becker J, Volk A, Kubisch C, Becker T, Kostic VS, Klein C, et al. Variants in the 3′UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression. Eur J Hum Genet. 2012;20(12):1265–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Blanckenberg J, Ntsapi C, Carr JA, Bardien S. EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson’s disease from South Africa. Neurobiol Aging. 2014;35(2):445.e441–3.

    Article  Google Scholar 

  22. Benitez BA, Jin SC, Guerreiro R, Graham R, Lord J, Harold D, Sims R, Lambert JC, Gibbs JR, Bras J, et al. Missense variant in TREML2 protects against Alzheimer’s disease. Neurobiol Aging. 2014;35(6):1510.e1519–26.

    Article  Google Scholar 

  23. Allen M, Kachadoorian M, Carrasquillo MM, Karhade A, Manly L, Burgess JD, Wang C, Serie D, Wang X, Siuda J, et al. Late-onset Alzheimer disease risk variants mark brain regulatory loci. Neurol Genet. 2015;1(2):e15.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Keogh MJ, Wei W, Wilson I, Coxhead J, Ryan S, Rollinson S, Griffin H, Kurzawa-Akanbi M, Santibanez-Koref M, Talbot K, et al. Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource. Genome Res. 2017;27(1):165–73.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Fogh I, Ratti A, Gellera C, Lin K, Tiloca C, Moskvina V, Corrado L, Soraru G, Cereda C, Corti S, et al. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Hum Mol Genet. 2014;23(8):2220–31.

    Article  CAS  PubMed  Google Scholar 

  26. Epilepsies ILAECoC. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. Lancet Neurol. 2014;13(9):893–903.

    Article  Google Scholar 

  27. Bettencourt C, Hensman-Moss D, Flower M, Wiethoff S, Brice A, Goizet C, Stevanin G, Koutsis G, Karadima G, Panas M, et al. DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Ann Neurol. 2016;79(6):983–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references


We are grateful to all the patients and their family members for participating in this study.


This research was supported by grants from the Tunisian Ministry of Higher Education and Scientific Research. Z.L has financial support within the framework of MOBIDOC Postdoc as specified in the PASRI program, funded by the European Union and managed by the ANPR.

Availability of data and materials

Data supporting the findings are included in the article. Any further information is available on request to the corresponding author.

Author information

Authors and Affiliations



RG is corresponding author and supervised the entire project. ZL, first author, conducted experiments and wrote the article, SB and HD assisted in the experiments. Study conception and design: ZL, RK, SA and CM. Patients follow-up: MB and AG-B. Data analysis and interpretation: ZL, MB, MD and SA. All authors have read and approved the final version of the manuscript.

Corresponding author

Correspondence to Riadh Gouider.

Ethics declarations

Ethics approval and consent to participate

Written informed consents were obtained from individuals before being enrolled in the genetic study. Research protocols were approved by the medical ethics committee of Razi Hospital and conformed to the guidelines of the Declaration of Helsinki.

Consent for publication

All participants included in this study signed a written informed consent for publication.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Landoulsi, Z., Benromdhan, S., Ben Djebara, M. et al. Using KASP technique to screen LRRK2 G2019S mutation in a large Tunisian cohort. BMC Med Genet 18, 70 (2017).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:


  • Parkinson’s disease
  • LRRK2 gene
  • G2019S
  • KASP
  • genetic testing