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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 abn...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Ferrata Storti Foundation
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2675680/ https://ncbi.nlm.nih.gov/pubmed/19286880 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2008.003301 |
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