Fig. 1From: Three novel mutations in the ATP7B gene of unrelated Vietnamese patients with Wilson diseaseMutations of the ATP7B gene were identified by sequencing in patient 1 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.Phe1026Tyr and heterozygous mutation c.2866-2A > GBack to article page