Bilirubin pigments were studied in the bile of 20 normal adults, 25 patients with Gilbert's syndrome, 9 children with Crigler-Najjar disease, and 6 patients with hemolysis, to determine how a deficiency of hepatic bilirubin UDP-glucuronosyltransferase would affect the end products of bilirubin biotransformation.
Johan Fevery, Norbert Blanckaert, Karel P. M. Heirwegh
Title and authors | Publication | Year |
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Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome
TY Shiu, HH Huang, HH Lin, YL Shih, HC Chu, WK Chang, TY Hsieh |
Liver International | 2015 |