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Article

Association of factor V Leiden and prothrombin gene mutation with Behçet's disease.

Archives of dermatological research - 1 Nov 2001

Tursen U, Kaya T I, Eskandari G, Gunduz O, Yazar M, Ikizoglu G, Atik U

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Share to Behcet Syndrome
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 11820731
DOI: 10.1007/pl00007469

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Association of factor V Leiden and prothrombin gene mutation with Behçet's disease.PMID 11820731Read ↗

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Factor V Leiden mutation and PAI-1 gene 4G/5G genotype in thrombotic patients with Behcet's disease.Semantic proximity Read ↗

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What is the clinical relevance of the prothrombin G20210A mutation?Semantic proximity Read ↗

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Association of allelic variants of factor V Leiden, prothrombin and methylenetetrahydrofolate reductase with thrombosis or ocular involvement in Behçet's disease: a systematic review and meta-analysis.Semantic proximity Read ↗

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