Fig. 1From: Coexistence of mutations of Gilbert’s syndrome and Crigler-Najjar syndrome in an infant with unconjugated hyperbilirubinemia—a case reportSequence chromatogram and alignment to the reference sequence showing the variation in exon 1 of the UGT1A1 gene (chr2:234669097A > G;c.164A > G;p.His55arg) detected in homozygous condition in the babyBack to article page