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Article

Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.

Genetics and molecular research : GMR - 28 Jan 2014

Hsieh T-Y, Shiu T-Y, Chu N-F, Chao T-Y, Chu H-C, Chang W-K, Chao Y-C, Huang H-H

Abstract excerpt

Gilbert's syndrome is suspected in patients with unconjugated hyperbilirubinemia caused by decreased activity of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene in the absence of abnormal liver function and hemolysis. The major genetic variants underlying Gilbert's syndrome are TATA-box repeats of the promoter region and exon 1 G211A of the coding region, particularly in Asians. The efficacy of DNA melting...

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Identifiers

PMID: 24615032
DOI: 10.4238/2014.January.28.12

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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