UGT1A1 gene mutation as a marker indicating there is a high risk of Gilbert's syndrome: Theoretical and applied aspects

UGT1A1 gene mutation as a marker indicating there is a high risk of Gilbert's syndrome: Theoretical and applied aspects

Gilbert's syndrome is a widely spread multi-factor pathology which is to a great extent genetically determined. Its basic etiological factor is lower activity of a liver enzyme, UDP-glucuronosyltransferase A1, caused by mutations in UGT1A1 gene. Functional disorders in the liver cause dyspepsia...

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Bibliographic Details
Main Authors: A.N. Volkov, E.V. Tsurkan
Format: Article
Language:English
Published: FBSI “Federal Scientific Center for Medical and Preventive Health Risk Management Technologies” 2019-06-01
Series:Analiz Riska Zdorovʹû
Subjects:
gilbert's syndrome
udp-glucuronosyltransferase а1
ugt1a1
rs8175347
mutations in a gene
genotype
molecular and genetic examination
Online Access:http://journal.fcrisk.ru/eng/2019/2/14

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