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Article

UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.

BioMed research international - 1 Jan 2018

Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M, Maskoen Ani M, Abdulhamied Lola I, Rahayuningsih Sri E, Asni Eni K, Sleutels Frank, Kockx Christel E M, van Ijcken Wilfred F J, Sukadi Abdurachman, Achmad Tri H

Abstract excerpt

Neonatal hyperbilirubinemia (NH) is a common finding in newborn babies in Indonesia. Common and rare variants of UGT1A1 have been known to contribute to NH etiology. This study aims to identify UGT1A1 genetic variation and haplotype associated with NH in Indonesian population. DNA was isolated from 116 cases and 115 controls and a targeted-deep sequencing approach was performed on the promoter, UTRs, and exonic...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 29607327
DOI: 10.1155/2018/9425843
PMCID: PMC5828093

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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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