Title : Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.

Pub. Date : 2005 Apr

PMID : 15771689






1 Functional Relationships(s)
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1 Recently, it was reported that the -3263T > G mutation in the phenobarbital response enhancer module in UGT1A1 was associated with the majority of cases of Gilbert syndrome. Phenobarbital UDP glucuronosyltransferase family 1 member A1 Homo sapiens