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Article: Research on prothrombin published by R. Bourouba et al.
- Article from:
- Blood Weekly
- Article date:
- November 12, 2009
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"The polymorphic mutation 677 C-T in the methylenetetrahydrofolate reductase (MTHFR) gene presents a heterogeneous worldwide distribution and is associated with different disorders such as cardiovascular disease. Its frequency shows great ethnic and geographic variations," scientists in Ankara, Turkey report (see also Prothrombin).
"The aim of this work is to determine the frequency of MTHFR 677 C-T and coexistence of MTHFR 677 C-T with 2 other common, hereditary thrombophilia causes-namely, factor V 1691 G-A and prothrombin (PT) 20210 G-A mutation-in the Setif region of Algeria. The study involved 147 apparently healthy participants (82 men and 65 women). ...