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Volumn 27, Issue 12, 2000, Pages 2849-2854
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Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothrombin gene G20210A mutations on deep venous thrombogenesis in Behcet's disease
a a a a a a a |
Author keywords
Behcet's disease; Deep venous thrombosis; Factor V leiden mutation; MTHFR C677T mutation; Prothrombin G20210A mutation
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Indexed keywords
5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);
BLOOD CLOTTING FACTOR 5 LEIDEN;
PROTHROMBIN;
ARTICLE;
BEHCET DISEASE;
CONTROLLED STUDY;
DEEP VEIN THROMBOSIS;
DISEASE ASSOCIATION;
DNA POLYMORPHISM;
FEMALE;
GENE MUTATION;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PRIORITY JOURNAL;
RISK ASSESSMENT;
THROMBOGENESIS;
TURKEY (REPUBLIC);
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
BEHCET SYNDROME;
FACTOR V;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MALE;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MIDDLE AGED;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
POINT MUTATION;
PROTHROMBIN;
RISK FACTORS;
VENOUS THROMBOSIS;
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EID: 0033668943
PISSN: 0315162X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (63)
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References (60)
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