Is a novel SCN3B mutation commonly found in SCN5A-negative brugada syndrome patients?

Circulation Journal

Volumn 77, Issue 4, 2013, Pages 900-901

  Kurakami, Kazuya ^a   Ishii, Kuniaki ^a  

^a YAMAGATA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE SENSITIVE POTASSIUM CHANNEL; CALCIUM CHANNEL L TYPE; SODIUM CHANNEL NAV1.5; VOLTAGE GATED SODIUM CHANNEL BETA 3 SUBUNIT;

BRUGADA SYNDROME; EDITORIAL; ELECTROPHYSIOLOGY; ENDOPLASMIC RETICULUM; GENE MUTATION; GENETIC SCREENING; HEART REPOLARIZATION; HEART RIGHT BUNDLE BRANCH BLOCK; HEART VENTRICLE FIBRILLATION; HUMAN; ION CURRENT; LOSS OF FUNCTION MUTATION; PHENOTYPE; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; ST SEGMENT ELEVATION; SUDDEN DEATH;

ANIMALS; BRUGADA SYNDROME; FEMALE; HUMANS; MALE; MUTATION, MISSENSE; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; VOLTAGE-GATED SODIUM CHANNEL BETA-3 SUBUNIT;

EID: 84875491715     PISSN: 13469843     EISSN: 13474820     Source Type: Journal    
DOI: 10.1253/circj.CJ-13-0242     Document Type: Editorial

References (15)

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