Effect of Genetic Variation in STXBP5 and STX2 on von Willebrand Factor and Bleeding Phenotype in Type 1 von Willebrand Disease Patients

BACKGROUND: In type 1 von Willebrand Disease (VWD) patients, von Willebrand Factor (VWF) levels and bleeding symptoms are highly variable. Recently, the association between genetic variations in STXBP5 and STX2 with VWF levels has been discovered in the general population. We assessed the relationsh...

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Main Authors: van Loon, Janine E., Sanders, Yvonne V., de Wee, Eva M., Kruip, Marieke J. H. A., de Maat, Moniek P. M., Leebeek, Frank W. G.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3391281/
https://ncbi.nlm.nih.gov/pubmed/22792389
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0040624
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