Fig. 2From: Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case reportModeling of the OCA2 protein. a p.Leu622. b p.Leu622Pro. c Structural representation of exons 17–21 deletion. Deleted residues are indicated in red and wild type residues are presented in blueBack to article page