Cellular and molecular basis of von Willebrand disease: studies on blood outgrowth endothelial cells

Von Willebrand disease (VWD) is a heterogeneous bleeding disorder caused by decrease or dysfunction of von Willebrand factor (VWF). A wide range of mutations in the VWF gene have been characterized; however, their cellular consequences are still poorly understood. Here we have used a recently develo...

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Detalhes bibliográficos
Main Authors: Starke, Richard D., Paschalaki, Koralia E., Dyer, Clare E. F., Harrison-Lavoie, Kimberly J., Cutler, Jacqueline A., McKinnon, Thomas A. J., Millar, Carolyn M., Cutler, Daniel F., Laffan, Mike A., Randi, Anna M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2013
Assuntos:
Thrombosis and Hemostasis
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3617637/
https://ncbi.nlm.nih.gov/pubmed/23355534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2012-06-435727
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