Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India
Author:
Funder
Council of Scientific and Industrial Reasearch (CSIR), India
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/article/10.1007/s11033-018-4305-6/fulltext.html
Reference21 articles.
1. Hirschfield GM, Alexander GJ (2006) Gilbert’s syndrome: an overview for clinical biochemists. Ann Clin Biochem 43:340–343
2. Farheen S, Sengupta S, Santra A, Pal S et al (2006) Gilbert’s syndrome: high frequency of the (TA) 7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene. World J Gastroenterol 12:2269–2275
3. Servedio V, D’Apolito M, Maiorano N et al (2005) Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. Hum Mutat 25:325–334
4. Beutler E, Gelbart T, Demina A (1998) Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci USA 95:8170–8174
5. Sugatani J, Yamakawa K, Yoshinari K et al (2002) Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia. Biochem Biophys Res Commun 292:492–497
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3. Factors Affecting Drug Metabolism;Human Drug Metabolism;2020-02-21
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