Fig. 2From: Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson diseaseMutations of the ATP7B gene were identified by sequencing in patient 2 and his family. Pedigree of patient’s family (a), the Kayser-Fleischer ring around the cornea of patient’s eye (b) and mutations (c) of ATP7B gene were identified, including a compound heterozygous mutation p.Ser105* and heterozygous frameshift mutation p.His251Alafs*19Back to article page