Allele-allele interaction within the F13A1 gene: A risk factor for Ischaemic Heart Disease in Spanish population

Thrombosis Research

Volumn 126, Issue 3, 2010, Pages

  Carreras Torres, Robert ^a   Athanasiadis, Georgios ^a   Via, Marc ^b   Trenchs, Joan ^a   Gayà Vidal, Magdalena ^a   Santamaria, Josep ^a   Esteban, Esther ^a   Moral, Pedro ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 13; FIBRINOGEN; MICROSATELLITE DNA;

ALLELE; BLOOD CLOTTING; BLOOD LEVEL; CARDIOVASCULAR RISK; CHROMOSOME 1Q; CHROMOSOME 6P; CONCENTRATION (PARAMETERS); CORONARY ARTERY DISEASE; EXON; FIBRINOLYSIS; GENE AMPLIFICATION; GENE FREQUENCY; GENE INTERACTION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; GENOTYPE ENVIRONMENT INTERACTION; HAPLOTYPE; ISCHEMIC HEART DISEASE; LETTER; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SPAIN;

ADULT; AGED; EUROPEAN CONTINENTAL ANCESTRY GROUP; FACTOR XIIIA; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; MYOCARDIAL ISCHEMIA; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK ASSESSMENT; RISK FACTORS; SPAIN;

EID: 77956267213     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.thromres.2010.04.021     Document Type: Letter

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