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Article

The molecular biology of von Willebrand disease.

Clinical and laboratory haematology - 1 Aug 2001

Keeney S, Cumming A M

Abstract excerpt

von Willebrand disease (VWD) is a common autosomally inherited bleeding disorder associated with mucosal or trauma-related bleeding in affected individuals. VWD results from either a quantitative or qualitative deficiency of von Willebrand factor (VWF)--a glycoprotein with essential roles in primary haemostasis and as a carrier of coagulation factor VIII (FVIII) in the circulation. In recent years the...

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Source

Identifiers

PMID: 11683782
DOI: 10.1046/j.1365-2257.2001.00400.x

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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