Fig. 3From: A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese familySanger sequencing chromatograms of the variant c.1183 + 1 G > C from each study participant. Arrows indicate the position of the nucleotide changes identified in this study. IV:1, V:2, and V:9 carried the variant. The variant was not detected in individuals IV:2, V:4, V:6, V:10, V:14, and VI:8Back to article page