PMID 17496722 2007 Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
PMID 11013440 2000 Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
PMID 9627603 1998 Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
PMID 7715297 1995 Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
PMID 17496722 2007 Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
PMID 9627603 1998 Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
PMID 11013440 2000 Several structural mutations of UGT1A1, for example, a G71R substitution, have been reported to cause mild reduction of UGT activity toward bilirubin, resulting in mild hyperbilirubinemia, consistent with Gilbert syndrome.
rs56059937 in
UGT1A3;UGT1A7;UGT1A5;UGT1A8;UGT1A9;UGT1A4;UGT1A6;UGT1A1;UGT1A10 gene and
Gilbert Disease (disorder)
PMID 11013440 2000 Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
PMID 9627603 1998 Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
PMID 17496722 2007 Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
PMID 12139570 2002 Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.