Probing rare von Willebrand disease–causing mutations in the D4 and C-domains of von Willebrand factor
Background: von Willebrand disease (VWD) is characterized by absence or reduction of plasma von Willebrand factor (VWF) levels or reduced protein function. While the spectrum of causative VWD mutations is vast, there has been limited characterization of variants occurring within the D4-C6 domains of...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2025-05-01
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| Colecção: | Research and Practice in Thrombosis and Haemostasis |
| Assuntos: | |
| Acesso em linha: | http://www.sciencedirect.com/science/article/pii/S2475037925002468 |
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