GILBERT’S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

GILBERT’S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

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Gilbert’s syndrome is a benign indirect hyperbilirubinemia of the hereditary nature, caused by deficiency of the enzyme uridindiphosphatglucuronitransferase. UGT1A1 gene is localized on chromosome 2q37. The most common is a defect in the promoter region of the gene pairs in the thymine-adenin. 200 c...

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Bibliographic Details
Main Authors:	I.N. Zakharova, M.I. Pykov, Z.V. Kaloeva, L.A. Kataeva, S.V. Shishkina, I.V. Berezhnaya, E.V. Reznichenko, N.V. Molotkova
Format:	Article
Language:	English
Published:	Paediatrician Publishers, LLC 2011-08-01
Series:	Pediatričeskaâ Farmakologiâ
Online Access:	https://pf.spr-journal.ru/jour/article/view/1253

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