Genetics of Brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes

Journal of Electrocardiology

Volumn 33, Issue , 2000, Pages 11-22

  Towbin, Jeffrey A ^a   Vatta, Matteo ^a   Li, Hua ^a  

^a TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

Arrhythmogenic right ventricular dysplasia; Brugada syndrome; Idiopathic ventricular fibrillation; Ion channels; Long QT syndrome; Potassium channel; Sodium channel

Indexed keywords

POTASSIUM CHANNEL; SODIUM CHANNEL;

ARRHYTHMOGENESIS; AUTOPSY; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; BRUGADA SYNDROME; CAUSE OF DEATH; CONFERENCE PAPER; DISEASE PREDISPOSITION; ELECTROCARDIOGRAM; GENE EXPRESSION; GENETIC ANALYSIS; HEART RIGHT VENTRICLE DYSPLASIA; HEART VENTRICLE FIBRILLATION; HUMAN; LONG QT SYNDROME; PRIORITY JOURNAL; T WAVE; UNITED STATES;

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA; BUNDLE-BRANCH BLOCK; DEATH, SUDDEN, CARDIAC; ELECTROCARDIOGRAPHY; HUMANS; ION CHANNELS; LONG QT SYNDROME; MUTATION; SYNDROME; VENTRICULAR FIBRILLATION;

EID: 0034472942     PISSN: 00220736     EISSN: None     Source Type: Journal    
DOI: 10.1054/jelc.2000.20361     Document Type: Article

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