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Article

Effects of the mutant von Willebrand factor gene in von Willebrand disease.

Human genetics - 1 Oct 1995

Zhang Z, Lindstedt M, Blombäck M, Anvret M

Abstract excerpt

Von Willebrand disease (vWD) is a common inherited bleeding disorder in humans, and can be divided into a mild (type 1) and severe (type 3) form. Previous linkage studies identified one subject with vWD type 1 who transmitted different alleles of the von Willebrand factor (vWF) gene to his two affected children, one having vWD type 3 and the other having type 1. By screening the promoter and coding sequence (52...

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Identifiers

PMID: 7557958
DOI: 10.1007/BF00191794

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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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Effects of the mutant von Willebrand factor gene in von Willebrand disease.PMID 7557958Read ↗

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Understanding von Willebrand's disease from gene defects to the patients.Semantic proximity Read ↗

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