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Von Willebrand disease - phenotype versus genotype: deficiency versus disease.

Thrombosis research - 1 Jan 2007

Lillicrap David

Abstract excerpt

Von Willebrand disease (VWD) is classified into three primary subtypes; type 1 includes partial quantitative deficiency, type 2 (A, B, M and N) includes qualitative defects and type 3 includes virtually complete deficiency of von Willebrand factor (VWF). Type 2A includes variants with decreased platelet adhesion caused by selective deficiency of high molecular weight VWF multimers. Type 2B includes variants with...

Topics

Genotype
Humans
Phenotype
von Willebrand Diseases
von Willebrand Factor

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17490730
DOI: 10.1016/j.thromres.2007.03.014

Genes

VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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