Fig. 2From: A novel homozygous TUB mutation associated with autosomal recessive retinitis pigmentosa in a consanguineous Chinese familyCo-segragation analysis of the c.1379A > G (p.Asn460SerSer) variant in TUB. A Sequences of the homozygous c.1379A > G variant in the proband (IV:4); B, C Sequences of the heterozygous carries (V:1, V:2) of the family; D Sequences of healthy member (IV:5) of the familyBack to article page