Diagnosis of gilbert’s syndrome via pyrosequencing in clinical practice
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caused by either impaired expression of the UGT1A1 gene, which encodes the isoform of the uridine-5-diphosphate glucuronosyltransferase (UDP-GTA1), or structural modifications of UDP-GTA1. GS is character...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Russo |
| Publicat: |
SINAPS LLC
2019-11-01
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| Col·lecció: | Архивъ внутренней медицины |
| Matèries: | |
| Accés en línia: | https://www.medarhive.ru/jour/article/view/987 |
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