Fig. 2From: Wilson disease, ABCC2 c.3972C > T polymorphism and primary liver cancers: suggestions from a familial clusterFamily pedigree. Type of diseases are shown in the legend. Black arrows show the two brothers with concomitant c.3972C > T SNP at exon 28 of ABCC2 gene, Wilson disease and primary liver malignancies. SNP: single nucleotide polymorphism; WD: Wilson disease; HCC: hepatocellular carcinoma; iCCA: intrahepatic cholangiocarcinomaBack to article page