Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

Figure 3

Sanger sequencing. Identification of c.2020G>T in the WFS1 gene in six affected individuals (II-2, III-2, III-10, III-8, III-12, and IV-3); it was absent in the unaffected individuals.