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Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family

BMC Medical Genetics volume 18, Article number: 99 (2017) Cite this article

The Original Article was published on 03 August 2017

Erratum

Following publication of the original article [1], the authors identified the following errors in the scientific content:

p.4, para. 3: “(1 tablet/10 mL RIPA)” should read “(1 tablet/10 mL RIPA buffer)”.

p.4, para. 4: “II-1” should read “II-2”.

Minor mistakes were also identified in the table on page 6, and in the Abbreviations section on page 7.

The original article has been corrected.

Reference

  1. Guarnieri V, Seaberg RM, Kelly C, Jean Davidson M, Raphael S, Shuen AY, Baorda F, Palumbo O, Scillitani A, Hendy GN, Cole DEC. Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family. BMC Med Genet. 2017;18:83. doi:10.1186/s12881-017-0445-0.

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Authors and Affiliations

  1. Medical Genetics, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy

    Vito Guarnieri, Filomena Baorda & Orazio Palumbo

  2. Department of Otolaryngology - Head and Neck Surgery, University of Toronto, Toronto, ON, Canada

    Raewyn M. Seaberg

  3. Department of Medicine, University of Toronto, Toronto, ON, Canada

    Catherine Kelly

  4. Division of Endocrinology, Women’s College Hospital, Toronto, ON, Canada

    Catherine Kelly

  5. Department of Otolaryngology, Head & Neck Surgery, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

    M. Jean Davidson

  6. Department of Anatomic Pathology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada

    Simon Raphael

  7. Departments of Laboratory Medicine and Pathobiology, Medicine and Genetics, University of Toronto, Toronto, ON, Canada

    Andrew Y. Shuen & David E.C. Cole

  8. Endocrinology, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy

    Alfredo Scillitani

  9. Metabolic Disorders and Complications, McGill University Health Centre-Research Institute, Montreal, QC, Canada

    Geoffrey N. Hendy

  10. Departments of Medicine, Physiology and Human Genetics, McGill University, Montreal, QC, Canada

    Geoffrey N. Hendy

Authors
  1. Vito Guarnieri
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  2. Raewyn M. Seaberg
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  3. Catherine Kelly
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  4. M. Jean Davidson
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  5. Simon Raphael
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  6. Andrew Y. Shuen
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  7. Filomena Baorda
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  8. Orazio Palumbo
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  9. Alfredo Scillitani
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  10. Geoffrey N. Hendy
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  11. David E.C. Cole
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Corresponding author

Correspondence to Vito Guarnieri.

Additional information

The online version of the original article can be found under doi:10.1186/s12881-017-0445-0

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Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), 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 (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Guarnieri, V., Seaberg, R.M., Kelly, C. et al. Erratum to: Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family. BMC Med Genet 18, 99 (2017). https://doi.org/10.1186/s12881-017-0459-7

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  • DOI: https://doi.org/10.1186/s12881-017-0459-7

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