Update on genetic analysis in Brugada syndrome

Heart Rhythm

Volumn 5, Issue 10, 2008, Pages 1495-1496

  Miura, Daiji ^a,b   Nakamura, Kazufumi ^a   Ohe, Tohru ^a,b  

^a OKAYAMA UNIVERSITY   (Japan)

^b Sakakibara Hospital   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADRENERGIC RECEPTOR; AJMALINE; CALCIUM CHANNEL L TYPE; CHOLINERGIC RECEPTOR; DELAYED RECTIFIER POTASSIUM CHANNEL; FLECAINIDE; GENOMIC DNA; ISOPRENALINE; PILSICAINIDE; PROCAINAMIDE; QUINIDINE; SODIUM CHANNEL;

ARRHYTHMOGENESIS; ARTICLE; BRUGADA SYNDROME; CLINICAL FEATURE; DEFIBRILLATOR; DIAGNOSTIC VALUE; DRUG EFFICACY; ELECTROCARDIOGRAM; FAMILY HISTORY; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE PHENOTYPE CORRELATION; HEART ATRIUM FIBRILLATION; HEART VENTRICLE FIBRILLATION; HUMAN; INCIDENCE; LONG QT SYNDROME; MUTATIONAL ANALYSIS; PATHOPHYSIOLOGY; PATIENT SELECTION; PENETRANCE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SINUS NODE DYSFUNCTION; ST SEGMENT ELEVATION; SUDDEN INFANT DEATH SYNDROME;

EID: 54549093729     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2008.07.026     Document Type: Note

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