Fig. 1From: A novel mutation in the PRPH2 gene in a Chinese pedigree with retinitis pigmentosa and angle-closure glaucomaPedigree of mainland Chinese Han family with inherited retinal degenerative disease. An autosomal dominant inheritance pattern is shown. Closed and open symbols indicate affected patients and unaffected subjects, respectively. The arrow indicates proband. A slash indicates that the individual is deceasedBack to article page