Double SCN5A mutation underlying asymptomatic Brugada syndrome

Heart Rhythm

Volumn 2, Issue 3, 2005, Pages 285-292

  Yokoi, Hisataka ^a   Makita, Naomasa ^a   Sasaki, Koji ^a   Takagi, Yasuhiro ^b   Okumura, Yasuo ^b   Nishino, Tetsuo ^c   Makiyama, Takeru ^d   Kitabatake, Akira ^a   Horie, Minoru ^e   Watanabe, Ichiro ^b   Tsutsui, Hiroyuki ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b NIHON UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c NTT CORPORATION   (Japan)

^d KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^e SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Asymptomatic mutation carrier; Brugada syndrome; Genetics; Patch clamp; SCN5A; Slow inactivation; Sodium channel; Ventricular fibrillation

Indexed keywords

BIOLOGICAL MARKER; FLECAINIDE; PILSICAINIDE; SODIUM CHANNEL; SODIUM ION;

ADULT; ALLELE; ARRHYTHMOGENESIS; ARTICLE; BRUGADA SYNDROME; CLINICAL ARTICLE; CONTROLLED STUDY; ECG ABNORMALITY; ELECTROSTIMULATION; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HEART ARRHYTHMIA; HEART VENTRICLE ARRHYTHMIA; HEART VENTRICLE FIBRILLATION; HUMAN; LETHALITY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; PROGNOSIS; PROVOCATION TEST; RISK ASSESSMENT; STEADY STATE; SUDDEN DEATH; SYNCOPE;

ARRHYTHMIA; BIOPHYSICS; BUNDLE-BRANCH BLOCK; ELECTROCARDIOGRAPHY; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; MUTATION, MISSENSE; SODIUM CHANNELS; SYNDROME;

EID: 20044374511     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2004.11.022     Document Type: Article

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