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Volumn 10, Issue 2, 1999, Pages 107-110

Thrombosis in a patient with combined homozygosity for the factor V Leiden mutation and a mutation in the 3'-untranslated region of the prothrombin gene

Author keywords

Thrombosis, mutation, factor V Leiden, prothrombin gene mutation

Indexed keywords

ANTICOAGULANT AGENT; BLOOD CLOTTING FACTOR 5; PROTHROMBIN; WARFARIN;

EID: 0033004944     PISSN: 09575235     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001721-199903000-00008     Document Type: Article
Times cited : (18)

References (12)
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  • 3
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    • Hypercoagulable states
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  • 6
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    • Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men
    • 6. Ridker PM, Hennekens CH, Lindpaintner K, Stampfer MJ, Eisenberg PR, Miletich JP. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Eng J Med 1995; 332: 912-917.
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  • 7
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    • The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis
    • 7. Hillarp A, Zöller B, Svensson P, Dahlbäck B. The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep vein thrombosis. Thromb Haemost 1997; 78: 990-992.
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    • Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.