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Article

A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns.

The Turkish journal of pediatrics - 1 Jan 2000

Ergin Hacer, Bican Mevlüt, Atalay O Erol

Abstract excerpt

The etiology of pathological jaundice can not be identified in almost half of the cases. The effect of promoter polymorphism in the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene was investigated in healthy breast-fed Turkish neonates with unexplained and direct Coombs'-negative ABO incompatible hyperbilirubinemia. Newborns whose peak serum bilirubin levels were > or = 17 mg/dl and < or = 12.9 mg/dl within the...

Read the complete abstract on PubMed

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Share to ABO gene
Share to Genotype
Share to Glucuronosyltransferase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperbilirubinemia, Neonatal

Share to Infant, Newborn

Share to Polymorphism, Genetic

Share to Promoter Regions, Genetic

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 20402064

Genes

ABO

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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