SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias

Journal of Cardiovascular Electrophysiology

Volumn 17, Issue 5, 2006, Pages 480-485

  Laitinen Forsblom, Päivi J ^a   Mäkynen, Pekka ^b   Mäkynen, Heikki ^b   Yli Mäyry, Sinikka ^b   Virtanen, Vesa ^b   Kontula, Kimmo ^a   Aalto Setälä, Katriina ^b,c  

^a UNIVERSITY OF HELSINKI   (Finland)

^b TAMPERE UNIVERSITY HOSPITAL   (Finland)

^c UNIVERSITY OF TAMPERE   (Finland)

Author keywords

Atrial arrhythmias; Cardiac conduction; Genetics; Pacemaker; SCN5A

Indexed keywords

ASPARAGINE; ASPARTIC ACID;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; APPARATUS; ARTICLE; ARTIFICIAL HEART PACEMAKER; BRADYCARDIA; BRAIN INFARCTION; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONTROLLED STUDY; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FAMILIAL DISEASE; FEMALE; FINLAND; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC MARKER; HEART ATRIUM ARRHYTHMIA; HEART FAILURE; HEART LEFT VENTRICLE SIZE; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; LINKAGE ANALYSIS; MALE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SCN5A GENE; STROKE; SUDDEN DEATH; SYMPTOMATOLOGY;

ATRIAL FIBRILLATION; BRADYCARDIA; COMORBIDITY; DNA MUTATIONAL ANALYSIS; FEMALE; FINLAND; GENETIC PREDISPOSITION TO DISEASE; HEART BLOCK; HUMANS; MALE; MUSCLE PROTEINS; MUTATION; PEDIGREE; PREVALENCE; RISK ASSESSMENT; RISK FACTORS; SODIUM CHANNELS;

EID: 33645965922     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2006.00411.x     Document Type: Article

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