Genetics of sudden death: Focus on inherited channelopathies

European Heart Journal

Volumn 32, Issue 17, 2011, Pages 2109-2120

  Cerrone, Marina ^a   Priori, Silvia G ^a,b,c  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b IRCCS   (Italy)

^c UNIVERSITY OF PAVIA   (Italy)

Author keywords

Channelopathies; Genetics; GWAS; Inherited arrhythmias; Sudden cardiac death

Indexed keywords

BRUGADA SYNDROME; CARDIAC CHANNELOPATHY; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CLINICAL FEATURE; CONGENITAL HEART DISEASE; ELECTROPHYSIOLOGY; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENOTYPE; HEART ARRHYTHMIA; HEART DISEASE; HEART MUSCLE POTENTIAL; HUMAN; INHERITED ARRHYTHMOGENIC DISEASE; LONG QT SYNDROME; PRIORITY JOURNAL; REVIEW; SHORT QT SYNDROME; SUDDEN DEATH;

ARRHYTHMIAS, CARDIAC; CARDIOMYOPATHIES; CHANNELOPATHIES; DEATH, SUDDEN, CARDIAC; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MUTATION; RISK FACTORS;

EID: 80052452464     PISSN: 0195668X     EISSN: 15229645     Source Type: Journal    
DOI: 10.1093/eurheartj/ehr082     Document Type: Review

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