Global prevalence of platelet-type von Willebrand disease
Background: Platelet-type von Willebrand disease (PT-VWD) is a rare autosomal dominant disorder. It is caused by gain-of-function gene variants in the platelet GP1BA, which results in excessive binding between GPIbα and von Willebrand factor (VWF). The prevalence of PT-VWD is unknown. Objectives: To...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2025-01-01
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| Colección: | Research and Practice in Thrombosis and Haemostasis |
| Materias: | |
| Acceso en línea: | http://www.sciencedirect.com/science/article/pii/S2475037925000068 |
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