Haplotypes on 9p21 modify the risk for coronary artery disease among Indians

DNA and Cell Biology

Volumn 30, Issue 2, 2011, Pages 105-110

  Ashokkumar, Manickaraj ^a   Emmanuel, Cyril ^b   Dhandapany, Perundurai S ^c,e   Rani, Deepa Selvi ^d   Saibabu, Ramineni ^a   Cherian, Kootturathu Mammen ^a   Thangaraj, Kumarasamy ^d  

^a International Centre for Cardio Thoracic and Vascular Diseases   (India)

^b Global Hospitals and Health City   (India)

^c MADURAI KAMARAJ UNIVERSITY   (India)

^d CENTRE FOR CELLULAR AND MOLECULAR BIOLOGY   (India)

^e MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CARDIOVASCULAR RISK; CHROMOSOME 9P; CONTROLLED STUDY; CORONARY ARTERY DISEASE; DISEASE COURSE; DNA FLANKING REGION; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; INDIAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK REDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOMES, HUMAN, PAIR 9; CORONARY ARTERY DISEASE; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INDIA; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 79551623339     PISSN: 10445498     EISSN: None     Source Type: Journal    
DOI: 10.1089/dna.2010.1046     Document Type: Article

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