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

Volumn 99, Issue 2, 2008, Pages 453-455

  Pecheniuk, Natalie M ^a   Elias, Darlene J ^a,b   Xu, Xiao ^a   Griffin, John H ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b SCRIPPS CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed 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; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN S; RECEPTOR, PAR-1; RECEPTORS, CELL SURFACE; REPRODUCIBILITY OF RESULTS; RESEARCH DESIGN; RISK ASSESSMENT; RISK FACTORS; SERINE ENDOPEPTIDASES; VENOUS THROMBOEMBOLISM;

EID: 38949217750     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160TH07-10-0607     Document Type: Letter

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