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Article

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.

Thrombosis and haemostasis - 1 Oct 2012

Yadegari Hamideh, Driesen Julia, Pavlova Anna, Biswas Arijit, Hertfelder Hans-Jörg, Oldenburg Johannes

Abstract excerpt

Von Willebrand disease (VWD) is the most common inherited bleeding disorder caused by quantitative or qualitative defects of the von Willebrand factor (VWF). VWD is classified into three types--type 1 (partial quantitative deficiencies), type 2 (qualitative defects) and type 3 (complete deficiency of VWF). In this study we explored genotype and phenotype characteristics of patients with VWD with the aim of...

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Identifiers

PMID: 22871923
DOI: 10.1160/TH12-02-0089

Genes

VWF

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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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