Impact of double heterozygosity for Factor V Leiden and Prothrombin G20210A on the thrombotic phenotype
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference27 articles.
1. Bauduer F, Lacombe D. Factor V Leiden, prothrombin 20210A, methylenetetrahydrofolate reductase 677T, and population genetics. Mol. Genet. Metab. 2005;86:91–99. doi: https://doi.org/10.1016/j.ymgme.2005.04.002.
2. Leroyer C, Mercier B, Escoffre M, Férec C, Mottier D. Factor V Leiden prevalence in venous thromboembolism patients. Chest 1997;111:1603–1606. doi: https://doi.org/10.1378/chest.111.6.1603.
3. The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis;Svensson;J. Intern. Med.,1997
4. 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
5. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels;Cattaneo;Thromb. Res.,1999
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