[Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].

doi:10.3760/cma.j.issn.1007-3418.2018.12.005

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Article

[Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology - 20 Dec 2018

Xiong Q F, Zhong Y D, Feng X N, Zhou H, Liu D X, Wu X P, Yang Y F

Abstract excerpt

Objective: To compare and analyze patient's general condition, changes in laboratory parameters, and the spectrum of UGT1A1 mutations in patients with inherited non-hemolytic unconjugated hyperbilirubinemia. Methods: A retrospective study was conducted at Nanjing Second Hospital from January 2015 to July 2018 and patients' demographic characteristics, liver function test, and UGT1A1 gene were analyzed. The...

Topics

Adult
Crigler-Najjar Syndrome
Female
Glucuronosyltransferase
Humans
Hyperbilirubinemia
Male
Middle Aged
Mutation
Retrospective Studies
Young Adult

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Identifiers

PMID: 30669781
DOI: 10.3760/cma.j.issn.1007-3418.2018.12.005
PMCID: PMC12769221

Genes

UGT1A1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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