Fig. 5From: A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese familySummary of all variants in the gene GSDME associated with hearing loss. Indicated are the 1 novel variant in the affected individuals in the family of this study (red font) and the 13 previously described variants (black font)Back to article page