Sanders, Y V <br/><br/>
CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease.  [electronic resource] 

 -  Journal of thrombosis and haemostasis : JTH  Jun 2015 
 - 956-66 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1538-7836 
<br/><br/><label>Standard No.: </label>10.1111/jth.12927  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Biomarkers--blood<br/>Blood Coagulation--genetics<br/>Blood Coagulation Tests<br/>Cell Adhesion Molecules--genetics<br/>Child<br/>Child, Preschool<br/>Cross-Sectional Studies<br/>Female<br/>Gene Frequency<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>Hemorrhage--blood<br/>Humans<br/>Infant<br/>Lectins, C-Type--genetics<br/>Male<br/>Middle Aged<br/>Molecular Diagnostic Techniques<br/>Nerve Tissue Proteins--genetics<br/>Netherlands<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>R-SNARE Proteins--genetics<br/>Receptors, Cell Surface--genetics<br/>Risk Factors<br/>Young Adult<br/>von Willebrand Disease, Type 1--blood<br/>von Willebrand Disease, Type 2--blood<br/>von Willebrand Factor--analysis