Figure 1From: Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis Pedigree of the Chinese family with three different UGT1A1 mutations. The proband is indicated by the arrow. The square represents the proband and his father and the circles represent the mother and the sister.Back to article page