Fig. 3From: Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case reportSanger sequencing traces showing the c.1924G>C; p.Asp642His mutation in exon 6 (upper row) and c.3809A>G; p.Asn1270Ser mutation in exon 18 (lower row) of the ATP7B gene. The segregation of these two mutations as compound heterozygote has been confirmed in six available DNA samples (two affected and four unaffected individuals) from this familyBack to article page