Genetic Spectrum ofUGT1A1in Korean Patients with Unconjugated Hyperbilirubinemia
Author:
Affiliation:
1. Department of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
2. Department of Laboratory Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
Publisher
Annals of Laboratory Medicine
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://synapse.koreamed.org/pdf/10.3343/alm.2020.40.3.281
Reference11 articles.
1. Polymorphisms in UDP Glucuronosyltransferase Genes: Functional Consequences and Clinical Relevance
2. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man.
3. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
4. Pharmacogenomics of human UDP-glucuronosyltransferase enzymes
5. A Case of Crigler-Najjar Syndrome Type 2 Diagnosed Using Genetic Mutation Analysis
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