Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference10 articles.
1. Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells;Ritter;J Biol Chem,1991
2. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini;Ritter;J Biol Chem,1992
3. Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyl- transferase gene complex with identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I;Bosma;Hepatology,1992
4. Identification of a genetic alteration in the code for bilirubin UDP-glucruronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type 1 patient.;Ritter;J Clin Invest,1992
5. Identifiation of defect in the genes of bilirubin UDP-glucruronosyltransferase in a patient with Crigler-Najjar syndrome type II;Aono;Biochem Biophys Res Commun,1993
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