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Genetic variants associated with deep vein thrombosis: the F11 locus
Journal of Thrombosis and Haemostasis, 10/27/09
Li Y et al. – Two SNPs, rs2289252 and rs2036914 in F11, appear to independently contribute to the risk of DVT, a contribution that is explained at least in part by an association with FXI levels.
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Today in Basic Science/Genetics...keeping you current
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Decreased expression of KLF6 and its significance in gastric carcinoma
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Today in Coagulation/Bleeding Dz...keeping you current
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