P.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, brugada syndrome, and atrial flutter

Journal of Cardiovascular Electrophysiology

Volumn 26, Issue 1, 2015, Pages 93-97

  Hothi, Sandeep S ^a,b,c   Ara, Farhana ^c,d   Timperley, Jonathan ^c  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^c NORTHAMPTON GENERAL HOSPITAL   (United Kingdom)

^d GLENFIELD HOSPITAL   (United Kingdom)

Author keywords

atrial flutter; Brugada syndrome; conduction disease; left bundle branch block; SCN5A; syncope

Indexed keywords

SODIUM CHANNEL NAV1.5; SCN5A PROTEIN, HUMAN;

ADULT; ARTICLE; BRUGADA SYNDROME; CASE REPORT; ELECTROCARDIOGRAM; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; HEART ATRIUM FLUTTER; HEART MUSCLE CONDUCTION DISTURBANCE; HEART VENTRICLE CONDUCTION; HUMAN; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR; MALE; PHENOTYPE; POLYMORPHIC VENTRICULAR TACHYCARDIA; PRIORITY JOURNAL; ADOLESCENT; ATRIAL FLUTTER; BUNDLE-BRANCH BLOCK; CHILD; ELECTROCARDIOGRAPHY; GENETIC PREDISPOSITION; GENETICS; HEART FUNCTION TEST; HEART MUSCLE CONDUCTION SYSTEM; HEREDITY; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PEDIGREE;

ADOLESCENT; ADULT; ATRIAL FLUTTER; BRUGADA SYNDROME; BUNDLE-BRANCH BLOCK; CHILD; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; ELECTROPHYSIOLOGIC TECHNIQUES, CARDIAC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEART CONDUCTION SYSTEM; HEREDITY; HUMANS; MALE; MIDDLE AGED; MUTATION; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PEDIGREE; PHENOTYPE;

EID: 84921559553     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/jce.12470     Document Type: Article

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