Is there a genetic basis for acute coronary syndrome? Commentary

Nature Clinical Practice Cardiovascular Medicine

Volumn 4, Issue 11, 2007, Pages 596-597

  Patay, Bradley A ^a   Topol, Eric J ^a  

^a SCRIPPS CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FIBRINOGEN; FIBRINOGEN BETA CHAIN; THROMBOSPONDIN 2; UNCLASSIFIED DRUG;

ACUTE CORONARY SYNDROME; DNA SEQUENCE; FAMILY HISTORY; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HEART INFARCTION; HUMAN; PRIORITY JOURNAL; PROMOTER REGION; RISK FACTOR; SHORT SURVEY; ST SEGMENT ELEVATION; UNSTABLE ANGINA PECTORIS;

EID: 35649017634     PISSN: 17434297     EISSN: 17434300     Source Type: Journal    
DOI: 10.1038/ncpcardio1006     Document Type: Short Survey

References (5)

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4. Chanock SJ et al. for the NCI-NHGRI Working Group on Replication in Association Studies (2007) Replicating genotype-phenotype associations. Nature 447: 655-660
5. Birney E et al. for the ENCODE Project Consortium (2007) Identification and analysis of functional elements in 1 % of the human genome by the ENCODE pilot project. Nature 447: 799-816