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Article

Variability in platelet- and collagen-binding defects in type 2M von Willebrand disease.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Jul 2013

Larsen D M, Haberichter S L, Gill J C, Shapiro A D, Flood V H

Abstract excerpt

Type 2M von Willebrand disease (VWD) includes qualitative defects in von Willebrand factor (VWF) function, with normal multimer distribution but a defect in VWF activity with respect to platelet or collagen binding. We characterized novel VWF gene mutations found in type 2M VWD subjects enrolled in the Zimmerman Program for the Molecular and Clinical Biology of VWD. Subjects were enrolled based on a pre-existing...

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Identifiers

PMID: 23496210
DOI: 10.1111/hae.12117
PMCID: PMC3688679

Genes

VWF

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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