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Article

Role of UGT1A1 mutation in fasting hyperbilirubinemia.

Journal of gastroenterology and hepatology - 1 Jun 2001

Ishihara T, Kaito M, Takeuchi K, Gabazza E C, Tanaka Y, Higuchi K, Ikoma J, Watanabe S, Sato H, Adachi Y

Abstract excerpt

BACKGROUND AND AIM: Low-grade fasting hyperbilirubinemia is a common observation in healthy subjects (HS), whereas high-grade fasting hyperbilirubinemia is believed to be a characteristic finding of Gilbert's syndrome. This study was undertaken to assess the role of mutation in bilirubin UDP- glycosyltransferase gene (UGT1A1) on fasting hyperbilirubinemia. METHODS: Analysis of UGT1A1 and a caloric restriction...

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Source

Identifiers

PMID: 11422622
DOI: 10.1046/j.1440-1746.2001.02495.x

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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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