Analysis of clinical and molecular genetic characteristics of Wiskott-Aldrich syndrome and X-linked thrombocytopenia
Introduction. Wiskott-Aldrich syndrome is a rare X-linked disorder characterized by microthrombocytopenia, eczema, and recurrent infections. It is caused by mutations of the WAS gene which encodes the WAS protein (WASp) – a key regulator of actin polymerization in hematopoietic cells. Mutations wit...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Asociatia de Biosiguranta si Biosecuritate
2021-06-01
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| Serie: | One Health & Risk Management |
| Soggetti: | |
| Accesso online: | https://journal.ohrm.bba.md/index.php/journal-ohrm-bba-md/article/view/141 |
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