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Article

Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism.

The Journal of pediatrics - 1 Jul 2014

Travan Laura, Lega Sara, Crovella Sergio, Montico Marcella, Panontin Elisa, Demarini Sergio

Abstract excerpt

OBJECTIVE: To assess whether UGT1A1 promoter polymorphisms associated with Gilbert Syndrome (GS) occur with a greater frequency in neonates with severe hyperbilirubinemia. STUDY DESIGN: In a case-control study performed at a single hospital center in Italy, 70 case subjects with severe hyperbilir...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 24726540
DOI: 10.1016/j.jpeds.2014.03.013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24726540-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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