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....
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| 格式: | 图书 |
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Union of pediatricians of Russia,
2011-08-01T00:00:00Z.
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A1234.567 |
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