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Article

Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.

Pediatrics international : official journal of the Japan Pediatric Society - 1 Aug 2009

Boo Nem-Yun, Wong Fei-Liang, Wang May-Kay, Othman Ainoon

Abstract excerpt

BACKGROUND: The aim of the present study was to compare, in a case-control study, the prevalence of nucleotide 211 guanine to adenine (G-->A) mutation of uridine diphosphoglucuronosyl transferase (UGT1A1) gene in Malaysian Chinese newborns with and without severe hyperbilirubinemia (total serum bilirubin >250 micromol/L during first 48 h of life or > or =300 micromol/L thereafter), and to determine whether this...

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Identifiers

PMID: 19674361
DOI: 10.1111/j.1442-200X.2008.02798.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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