Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease
Objectives MYH9-related disease (MYH9-RD) is a congenital bleeding disorder characterized by thrombocytopenia, platelet macrocytosis, inclusion bodies in neutrophils.The aim of this study was to investigate a Chinese family with MYH9-RD and to identity potential mutations of the MYH9. This investiga...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Taylor & Francis Group
2025-12-01
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| Col·lecció: | Hematology |
| Matèries: | |
| Accés en línia: | https://www.tandfonline.com/doi/10.1080/16078454.2025.2532923 |
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