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

Abstract

The -3263T > G mutation is not likely to be associated with the neonatal hyperbilirubinemia in Japanese.