Common variants for atrial fibrillation: Results from genome-wide association studies

Human Genetics

Volumn 131, Issue 1, 2012, Pages 33-39

  Liu, Xinyuan ^a   Wang, Fei ^a   Knight, Ashley C ^b   Zhao, Jiangmin ^a   Xiao, Junjie ^a,b  

^a TONGJI UNIVERSITY   (China)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR PIT 1; TRANSCRIPTION FACTOR PITX2; ZINC FINGER PROTEIN;

BRAIN ISCHEMIA; CARDIOVASCULAR RISK; CELL DIFFERENTIATION; CELL GROWTH; CHINESE; CHROMOSOME 16Q; CHROMOSOME 1Q; CHROMOSOME 4Q; CORONARY ARTERY BYPASS GRAFT; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HEART ATRIUM FIBRILLATION; HEART ATRIUM FLUTTER; HEREDITY; HUMAN; MOLECULAR BIOLOGY; POSTOPERATIVE PERIOD; PRIORITY JOURNAL; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; STROKE;

ATRIAL FIBRILLATION; GENES; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84856640406     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-011-1052-3     Document Type: Review

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