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Article

Vascular behcet and mutations in thrombogenic genes: methylene tetrahydrofolate reductase, factor V, and prothrombin.

Genetic testing and molecular biomarkers - 1 Jan 2012

Dagan Efrat, Baruch Yoav, Fiorilli Massimo, Rozenbaum Michael, Rosner Itzhak, Gershoni-Baruch Ruth

Abstract excerpt

Vasculitis, thrombophlebitis, arterial aneurysms, and occlusions occur in about 25% of patients with Behçet's disease (BD). The common inherited gene defects, factor V (FV) 1691A (Leiden), methylene tetrahydrofolate reductase (MTHFR) 677T, and prothrombin 20210A, are known risk factors for thrombosis. The aim of the study was to evaluate the contribution of these mutations to thrombosis in Israeli patients with...

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Source

Identifiers

PMID: 21861708
DOI: 10.1089/gtmb.2011.0096

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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