Rawa, Katarzyna and Adamowicz-Salach, Anna and Matysiak, Michal and Trzemecka, Anna and Burzynska, Beata (2012) Coexistence of Gilbert syndrome with hereditary haemolytic anaemias. Journal of clinical pathology, 65 (7). pp. 663-5. ISSN 1472-4146
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Abstract
Genotyping of the UGT1A1 gene showed distinct distribution of the common A(TA)(n)TAA polymorphism relative to other European populations. Because of a greater risk of hyperbilirubinaemia due to hereditary haemolytic anaemia, the diagnosis of Gilbert syndrome in this group of patients is very important.
| Item Type: | Article |
|---|---|
| Subjects: | Q Science > QH Natural history > QH426 Genetics R Medicine > R Medicine (General) |
| Divisions: | Department of Genetics |
| ID Code: | 472 |
| Deposited By: | Dr Beata Burzynska |
| Deposited On: | 11 Mar 2013 08:24 |
| Last Modified: | 11 Mar 2013 08:24 |
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