GILBERT’S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

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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Auteurs principaux:	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:	Artigo
Langue:	Russo
Publié:	Union of pediatricians of Russia 2011-08-01
Collection:	Педиатрическая фармакология
Accès en ligne:	https://www.pedpharma.ru/jour/article/view/1253
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