Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.

von Willebrand disease (vWD), the most common inherited bleeding disorder in humans, can result from either a quantitative or a qualitative defect in the adhesive glycoprotein, von Willebrand factor (vWF). Molecular studies of vWD have been limited by the large size of the vWF gene and difficulty in...

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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Ginsburg, D, Konkle, B A, Gill, J C, Montgomery, R R, Bockenstedt, P L, Johnson, T A, Yang, A Y
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1989
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC287212/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2786201/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.10.3723
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