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[Study on genetic mutations of the vWF in type 2A von Willebrand disease].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Aug 2000

Wang Y, Zhang J, Zhang W, Cheng D, Wan H, Ruan C

Abstract excerpt

OBJECTIVE: To study the molecular pathological mechanism of the type 2A von Willebrand disease(vWD) and the relationship of the phenotypes with genotypes. METHODS: A total of 126 patients with the hereditary hemorrhagic disease were examined using bleeding time, vWF:Ag, FVIII:CAg, ristocentin ind...

Topics

Adolescent
Adult
Female
Humans
Male
Middle Aged
Mutation
Polymerase Chain Reaction
von Willebrand Diseases
von Willebrand Factor

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10932002

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026. Prepared record publication-10932002-2026-08-31.1. Manifest publication-graph-cohort-2026-08-31.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 31 Aug 2026.

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