Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr).

Reports of families with members affected with both von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia (HHT) suggest a possible relationship between these two disorders. vWD, the most common inherited bleeding disorder in humans, is due to either a quantitative or qualitative def...

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Detalhes bibliográficos
Main Authors: Iannuzzi, M C, Hidaka, N, Boehnke, M, Bruck, M E, Hanna, W T, Collins, F S, Ginsburg, D
Formato: Artigo
Idioma:Inglês
Publicado em: 1991
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682950/
https://ncbi.nlm.nih.gov/pubmed/1673047
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