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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....

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Bibliografski detalji
Glavni autori:	I.N. Zakharova (Autor), M.I. Pykov (Autor), Z.V. Kaloeva (Autor), L.A. Kataeva (Autor), S.V. Shishkina (Autor), I.V. Berezhnaya (Autor), E.V. Reznichenko (Autor), N.V. Molotkova (Autor)
Format:	Knjiga
Izdano:	Union of pediatricians of Russia, 2011-08-01T00:00:00Z.
Teme:	article
Online pristup:	Connect to this object online.
Oznake:	Dodaj oznaku Bez oznaka, Budi prvi tko označuje ovaj zapis!

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