CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease. [electronic resource]
Producer: 20160225Description: 956-66 p. digitalISSN:- 1538-7836
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Biomarkers -- blood
- Blood Coagulation -- genetics
- Blood Coagulation Tests
- Cell Adhesion Molecules -- genetics
- Child
- Child, Preschool
- Cross-Sectional Studies
- Female
- Gene Frequency
- Genetic Association Studies
- Genetic Predisposition to Disease
- Hemorrhage -- blood
- Humans
- Infant
- Lectins, C-Type -- genetics
- Male
- Middle Aged
- Molecular Diagnostic Techniques
- Nerve Tissue Proteins -- genetics
- Netherlands
- Phenotype
- Polymorphism, Single Nucleotide
- R-SNARE Proteins -- genetics
- Receptors, Cell Surface -- genetics
- Risk Factors
- Young Adult
- von Willebrand Disease, Type 1 -- blood
- von Willebrand Disease, Type 2 -- blood
- von Willebrand Factor -- analysis
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Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
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