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Fig. 1 | BMC Medical Genetics

Fig. 1

From: A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing

Fig. 1

The pedigree for USH2C in Chinese with consanguineous marriage. Family numbers and disease-causing variant is noted above pedigree. Normal individuals are shown as clear circles (females) and squares (males), whereas affected individual is shown as a filled symbol. III:1 and III:2 are consanguineous marriage with symbol “=”. The patient above the arrow indicates the proband (IV:1). The arrow indicates the patient by next generation sequencing with G duplication mutation of GPR98 gene NM_032119.3: c.6912dupG: p.Leu2305Valfs*4. “M” indicates the mutant allele of GPR98, whereas “N” indicates normal allele without mutation

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BMC Medical Genetics

ISSN: 1471-2350

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