Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference17 articles.
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3. Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I;Bosma;Hepatology,1992
4. Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II;Aono;Biochem Biophys Res Commun,1993
5. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome;Bosma;N Engl J Med,1995
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