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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391281/
https://www.ncbi.nlm.nih.gov/pubmed/22792389
http://dx.doi.org/10.1371/journal.pone.0040624

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391281/
https://www.ncbi.nlm.nih.gov/pubmed/22792389
http://dx.doi.org/10.1371/journal.pone.0040624

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