Autosomal dominant C1149R von Willebrand disease: phenotypic findings and their implications
Background Mutation C1149R in the von Willebrand factor (VWF) gene has been thought to cause autosomal dominant severe type 1 von Willebrand disease (VWD).Design and Methods Eight patients from three unrelated families with this mutation were included in the present study who had distinct VWF abnorm...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2009-05-01
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| coleção: | Haematologica |
| Acesso em linha: | https://haematologica.org/article/view/5246 |
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