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Article

Impact of thrombogenic mutations on clinical phenotypes of von Willebrand disease.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis - 1 Jun 2010

Ahmad Firdos, Kannan Meganathan, Yadav Vinita, Biswas Arijit, Saxena Renu

Abstract excerpt

von Willebrand disease (VWD) is a most common inherited bleeding disorder. von Willebrand factor (VWF) exists as an extracellular adaptor molecule and generally involves in the hemostasis mechanism through binding with GP (Glycoprotein) Ib-IX-V platelet receptor. Clinical phenotype of bleeding di...

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Source

Identifiers

PMID: 19959486
DOI: 10.1177/1076029609351291

Genes

MTHFR
VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19959486-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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