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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
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.
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2012
Teme:
Research Article
Online dostop: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
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki