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Fig. 3 | BMC Medical Genetics

Fig. 3

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

Fig. 3

Validation and segregation analysis by Sanger sequencing. a, b, c and d indicate the sequencing results in III: 1 (M204, heterozygous type), III: 2 (heterozygous type), IV: 1 (M203, mutant homozygous type) and IV:2 (wild type, normal control: no eye and ear disease history in her family), respectively. The arrows indicate the duplication at the nucleotide position for GPR98 gene NM_032119.3: c.6912dupG: p.Leu2305Valfs*4

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BMC Medical Genetics

ISSN: 1471-2350

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