Short QT syndrome: Genotype-phenotype correlations

Journal of Electrocardiology

Volumn 38, Issue 4 SUPPL., 2005, Pages 75-80

  Borggrefe, Martin ^a   Wolpert, Christian ^a   Antzelevitch, Charles ^c   Veltmann, Christian ^a   Giustetto, Carla ^b   Gaita, Fiorenzo ^b   Schimpf, Rainer ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b Ospedale Civile di Asti   (Italy)

^c MASONIC MEDICAL RESEARCH LABORATORY   (United States)

Author keywords

Atrial fibrillation; Mutation; Repolarization; Short QT syndrome; Sudden death; Ventricular tachyarrhythmias

Indexed keywords

FLECAINIDE; IBUTILIDE; POTASSIUM CHANNEL HERG; POTASSIUM CHANNEL KCNQ1; PROPAFENONE; QUINIDINE; SOTALOL;

AGE DISTRIBUTION; CARDIOVASCULAR RISK; CLINICAL FEATURE; CONFERENCE PAPER; CONGENITAL HEART DISEASE; DEFIBRILLATOR; ECG ABNORMALITY; EXTRASYSTOLE; FAMILY HISTORY; GENOTYPE PHENOTYPE CORRELATION; HEART ATRIUM FIBRILLATION; HEART MUSCLE CONDUCTION DISTURBANCE; HEART REPOLARIZATION; HEART VENTRICLE TACHYCARDIA; HUMAN; MEDICAL ASSESSMENT; PRIORITY JOURNAL; QT DISPERSION; QT INTERVAL; REENTRY ARRHYTHMIA; SHORT QT SYNDROME; SUDDEN DEATH; SYNCOPE;

ANTI-ARRHYTHMIA AGENTS; ARRHYTHMIA; DEFIBRILLATORS, IMPLANTABLE; ELECTROCARDIOGRAPHY; GENOTYPE; HEART CONDUCTION SYSTEM; HUMANS; PHENOTYPE; QUINIDINE;

EID: 26444448370     PISSN: 00220736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jelectrocard.2005.06.009     Document Type: Conference Paper

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