GILBERT'S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

GILBERT'S SYNDROME IN CHILDREN: CONTEMPORARY DIAGNOSTIC POTENTIALITIES

Show other versions (1)

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....

Full description

Saved in:
Bibliographic Details
Main Authors: I.N. Zakharova (Author), M.I. Pykov (Author), Z.V. Kaloeva (Author), L.A. Kataeva (Author), S.V. Shishkina (Author), I.V. Berezhnaya (Author), E.V. Reznichenko (Author), N.V. Molotkova (Author)
Format: Book
Published: Union of pediatricians of Russia, 2011-08-01T00:00:00Z.
Subjects:
article
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available

Similar Items