Genetic testing of <scp> <i>UGT1A1</i> </scp> in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population-Reference-Cited by-同舟云学术

Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population

Published:2022-04-14 Issue:7 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Gu Leilei¹^ORCID,Han Yue²,Zhang Donghua²,Gong Qiming²,Zhang Xinxin²³^ORCID

Affiliation:

1. Department of Gastroenterology, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

2. Research Laboratory of Clinical Virology, Department of Infectious Diseases, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

3. Clinical Research Center, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1958

Reference21 articles.

1. UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children

2. Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

3. Gilbert and Crigler Najjar syndromes: An update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database

4. Interindividual variability in acetaminophen glucuronidation by human liver microsomes: Identification of relevant acetaminophen UDP‐glucuronosyltransferase isoforms;Court M. H.;The Journal of Pharmacology and Experimental Therapeutics,2001

5. Gilbert’s syndrome: High frequency of the (TA)7TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene

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