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TA-insertion mutation in bilirubin-UDP glucuronosyltransferase gene (UGT1A1) promoter in Indian patients with Gilbert's syndrome

✍ Scribed by M.K. Parvez; A. Goyal; N. Kazim; S.E. Hasnain; S.K. Sarin


Book ID
118565493
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
225 KB
Volume
36
Category
Article
ISSN
0168-8278

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Gilbert's syndrome, due to reduced hepatic bilirubin glucuronidation is associated with the presence of two extra nucleotides (TA) in the promoter region of the UDP-glucuronosyltransferase 1 (UGT1A1) gene. A rapid method was developed to detect this genetic polymorphism, using double gradient denatu