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Failure to validate association of gene polymorphisms in EPCR, PAR-1, FSAP and protein S Tokushima with venous thromboembolism among Californians of European ancestry [3]

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 [3]. Thrombosis and Haemostasis, 99(2), pp. 453-455.

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ID Code: 43497
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
DOI: 10.1160/TH07-10-0607
ISSN: 0340-6245
Divisions: Current > Institutes > Institute of Health and Biomedical Innovation
Copyright Owner: Schattauer
Deposited On: 22 Jul 2011 16:45
Last Modified: 25 Jul 2011 13:51

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