Failure to validate association of gene polymorphisms in EPCR, PAR-1, FSAP and protein S Tokushima with venous thromboembolism among Californians of European ancestry 
Pecheniuk, N. M., Elias, D. J. , Xu, X. , & Griffin, J. H. (2008) Failure to validate association of gene polymorphisms in EPCR, PAR-1, FSAP and protein S Tokushima with venous thromboembolism among Californians of European ancestry . Thrombosis and Haemostasis, 99(2), pp. 453-455.
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|Item Type:||Journal Article|
|Keywords:||blood clotting factor, endothelial protein C receptor, factor vii activating protease, protein C, protein S, proteinase activated receptor 1, thrombin, thrombomodulin, unclassified drug, DNA polymorphism, European American, gene deletion, gene frequency, gene insertion, genotype, human, letter, priority journal, venous thromboembolism, Antigens, CD, California, Case-Control Studies, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Humans, Male, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Receptor, PAR-1, Receptors, Cell Surface, Reproducibility of Results, Research Design, Risk Assessment, Risk Factors, Serine Endopeptidases|
|Divisions:||Current > Institutes > Institute of Health and Biomedical Innovation|
|Deposited On:||22 Jul 2011 16:45|
|Last Modified:||25 Jul 2011 13:51|
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