Ten years of genes in inherited arrhythmia syndromes: An example of what we have learned from patients, electrocardiograms, and computers

Journal of Electrocardiology

Volumn 38, Issue 4 SUPPL., 2005, Pages 145-149

  Wilde, Arthur A M ^a   Van Den Berg, Maarten P ^b  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

BRADYCARDIA; BRUGADA SYNDROME; CARDIOLOGY; COMPUTER MODEL; CONFERENCE PAPER; DIAGNOSTIC ACCURACY; ELECTROCARDIOGRAM; GENE MUTATION; HEART ARRHYTHMIA; HEART ELECTROPHYSIOLOGY; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; INCIDENCE; INHERITANCE; MOLECULAR GENETICS; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; QT PROLONGATION; SINUS NODE DYSFUNCTION; ST SEGMENT ELEVATION; SUDDEN DEATH;

ARRHYTHMIA; ELECTROCARDIOGRAPHY; ELECTROCARDIOGRAPHY, AMBULATORY; GENETIC PREDISPOSITION TO DISEASE; HEART CONDUCTION SYSTEM; HUMANS; MUTATION; SIGNAL PROCESSING, COMPUTER-ASSISTED; SODIUM CHANNELS; SYNDROME;

EID: 26444496486     PISSN: 00220736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jelectrocard.2005.06.103     Document Type: Conference Paper

References (12)

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