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Article

Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation.

Thrombosis and haemostasis - 1 Sept 1999

Castaman G, Eikenboom J C, Bertina R M, Rodeghiero F

Abstract excerpt

In a previous epidemiological investigation among schoolchildren of Northern Italy, a conservative 1% prevalence of type 1 von Willebrand disease (VWD) was found. Diagnosis was based on a positive family history and low von Willebrand factor (VWF) ristocetin cofactor activity. To investigate whether the type 1 VWD phenotype as detected by our original methodology cosegregates with one or more specific alleles of...

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Source

Identifiers

PMID: 10494765

Genes

VWF

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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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Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation.PMID 10494765Read ↗

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