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Article

Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.

Journal of biomedical science - 1 Jan 2005

Huang Ching-Shan

Abstract excerpt

In bilirubin metabolism, increased destruction of erythrocytes, defect in the function of organic anion transporter polypeptide 2 (OATP2) or UDP-glucuronosyltransferase 1A1 (UGT1A1) may result in unconjugated hyperbilirubinemia. Although glucose-6-phosphate dehydrogenase (G6PD) deficiency is known to be associated with the development of neonatal hyperbilirubinemia, it was observed that in neonates severe...

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Source

Identifiers

PMID: 15965581
DOI: 10.1007/s11373-005-3863-5

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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