An Arab selective gradient in the distribution of factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase (MTHFR) C677T
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2005.01546.x/fullpdf
Reference12 articles.
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2. 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
3. Methylenetetrahydrofolate reductase C677T genotype and venous thrombo-embolic disease;Couturaud;Respiration,2000
4. Prevalence of two thrombophilia predisposing mutations: factor V G1691A (R506Q; Leiden) and prothrombin G20210A, among healthy Lebanese;Tamim;Thromb Haemost,2002
5. Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant;Arnutti;Southeast Asian J Trop Med Public Health,2002
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