Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

Circulation

Volumn 104, Issue 25, 2001, Pages 3081-3086

  Kyndt, Florence ^a,b   Probst, Vincent ^a,b   Potet, Franck ^a,b   Demolombe, Sophie ^a,b   Chevallier, Jean Christophe ^a,b   Baro, Isabelle ^a,b   Moisan, Jean Paul ^a,b   Boisseau, Pierre ^a,b   Schott, Jean Jacques ^a,b   Escande, Denis ^a,b   Le Marec, Hervé ^a,b,c  

^a HÔTEL DIEU   (France)

^b CHU de Nantes   (France)

^c INSERM   (France)

Author keywords

Arrhythmia; Bundle branch block; Fibrillation; Genetics; Heart block

Indexed keywords

ARGININE; FLECAINIDE; GLYCINE; SODIUM CHANNEL;

ALPHA CHAIN; ARTICLE; BRUGADA SYNDROME; CLINICAL FEATURE; DEFIBRILLATOR; DISEASE COURSE; FAMILY STUDY; FEMALE; FRANCE; HEART ELECTROPHYSIOLOGY; HEART MUSCLE CONDUCTION DISTURBANCE; HEART RIGHT BUNDLE BRANCH BLOCK; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; ST SEGMENT ELEVATION;

EID: 0035909898     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/hc5001.100834     Document Type: Article

References (21)

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