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Article

Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals.

Journal of gastrointestinal and liver diseases : JGLD - 1 Mar 2017

Radoi Viorica E, Ursu Radu I, Poenaru Elena, Arsene Cosmin, Bohiltea Camil L, Bohiltea Roxana

Abstract excerpt

BACKGROUND AND AIMS: Gilbert syndrome (GS) is characterized by unconjugated hyperbilirubinemia without liver disease or overt hemolysis and it is found in 3-10% of the general population. Inherited hyperbilirubinaemia is attributable to a reduced UGT1A1 activity. The UGT1A1 promoter (TA) repeats variants are documented of being involved in abnormally elevated bilirubin levels. The aim of the present study is to...

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Source

Identifiers

PMID: 28338110
DOI: 10.15403/jgld.2014.1121.261.ugt

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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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