Fig. 3From: A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2Mutation detection and conservation analysis. a ~ h The sanger sequence results of the family members; i Protein alignment shows conservation of the G296 residue of KNCQ4 across 15 speciesBack to article page