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Article

Two novel mutations identified in a type 3 von Willebrand disease patient.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Dec 2014

Ouyang Wanyan, Yu Ziqiang, Yin Jie, Su Jian, Yang Chunchen, Ruan Changgeng

Abstract excerpt

von Willebrand disease (VWD) is the most common inherited bleeding disorder in humans. Caused by mutations in the von Willebrand factor (VWF) gene, these defects result in qualitatively abnormal variants of VWF (classi&filig;ed as type 2 VWD) or a decrease in VWF levels (types 1 and 3 VWD). Type...

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Identifiers

PMID: 24914743
DOI: 10.1097/MBC.0000000000000157

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VWF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24914743-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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