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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Bibliografiska uppgifter
Huvudupphovsmän: Ginsburg, D, Konkle, B A, Gill, J C, Montgomery, R R, Bockenstedt, P L, Johnson, T A, Yang, A Y
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1989
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC287212/
https://ncbi.nlm.nih.gov/pubmed/2786201
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