Figure 3From: Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa Identification of the homozygous mutation in the consanguineous Chinese arRP family. A and B show the exon 26 of EYS sequences from a normal individual and an affected individual with p.E1836X mutation, respectively. The sequence for individual III1, who is heterozygous for the mutation, is shown in C.Back to article page