Prothrombin G20210A mutation, antithrombin, heparin cofactor II, protein C, and protein S defects
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology
Reference160 articles.
1. A common genetic variation in the 3′-untranslated region of the Prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis;Poort;Blood,1996
2. Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'-untranslated region of the Prothrombin gene;Brown;Br J Haematol,1997
3. Geographic distribution of the 20210G to A Prothrombin variant;Rosendaal;Thromb Haemost,1998
4. The heterozygous 20210 G/A Prothrombin genotype is associated with early venous thrombosis in inherited thrombophilia and is not increased in frequency in arterial disease;Ferraresi;Atherosclerosis Thrombosis Vascular Biology,1997
5. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients;De Stefano;Blood,1998
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