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Article

Platelet-type von Willebrand disease: new insights into the molecular pathophysiology of a unique platelet defect.

Seminars in thrombosis and hemostasis - 1 Sept 2013

Othman Maha, Kaur Harmanpreet, Emsley Jonas

Abstract excerpt

Compared with coagulation factor defects, little attention is given to defects of platelet function as causes of rare bleeding disorders. Platelet-type von Willebrand disease (PT-VWD) is an autosomal dominant bleeding disorder and is unique among platelet disorders because it is characterized by platelet hyperresponsiveness rather than decreased function. The disease is caused by gain-of-function mutations in the...

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Source

Identifiers

PMID: 23934752
DOI: 10.1055/s-0033-1353442

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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Platelet-type von Willebrand disease: new insights into the molecular pathophysiology of a unique platelet defect.PMID 23934752Read ↗

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