Brugada syndrome with marked conduction disease: Dual implications of a SCN5A mutation

PACE - Pacing and Clinical Electrophysiology

Volumn 31, Issue 5, 2008, Pages 630-634

  Vorobiof, Gabriel ^a,c   Kroening, Daniel ^a   Hall, Burr ^a   Brugada, Ramon ^b   Huang, David ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b MONTREAL HEART INSTITUTE   (Canada)

^c NONE   (United States)

Author keywords

Defibrillation ICD; Electrophysiology clinical

Indexed keywords

SODIUM CHANNEL; SODIUM CHANNEL SCN5A;

ADULT; ARTICLE; ATRIOVENTRICULAR BLOCK; BRUGADA SYNDROME; CASE REPORT; CLINICAL FEATURE; DEFIBRILLATOR; ELECTROCARDIOGRAPHY; FAMILY STUDY; FEMALE; FOLLOW UP; GENETIC ANALYSIS; HEART ELECTROPHYSIOLOGY; HEART MUSCLE CONDUCTION DISTURBANCE; HEART VENTRICLE FIBRILLATION; HUMAN; IMPLANTATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; POLYMORPHIC VENTRICULAR TACHYCARDIA; SYNCOPE;

ATRIOVENTRICULAR BLOCK; BRUGADA SYNDROME; DEFIBRILLATORS, IMPLANTABLE; DIAGNOSIS, DIFFERENTIAL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MIDDLE AGED;

EID: 42649135859     PISSN: 01478389     EISSN: 15408159     Source Type: Journal    
DOI: 10.1111/j.1540-8159.2008.01056.x     Document Type: Article

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