Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: Correlation of genotype to phenotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference75 articles.
1. Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II
2. A New Type of Defect in the Gene for Bilirubin Uridine 5 '-Diphosphate-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type I
3. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
4. CHRONIC UNCONJUGATED HYPERBILIRUBINEMIA WITHOUT OVERT SIGNS OF HEMOLYSIS IN ADOLESCENTS AND ADULTS*
5. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency
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