Fig. 3From: Novel compound heterozygous mutations in OCA2 gene associated with non-syndromic oculocutaneous albinism in a Chinese Han patient: a case reportConfirmation of two mutations by Sanger sequencing. a OCA2 NM_000275: c.1865 T > C (p.Leu622Pro). b MYO7 NM_000260: c.4805G > A (p.Arg1602Gln)Back to article page