Inherited arrhythmia syndromes: Exome sequencing opens a new door to diagnosis

Journal of the American College of Cardiology

Volumn 63, Issue 3, 2014, Pages 267-268

  Chugh, Sumeet S ^a   Huertas Vazquez, Adriana ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

calmodulin; genetics; idiopathic ventricular fibrillation; ventricular arrhythmia; whole exome sequencing

Indexed keywords

CALM1 GENE; CALM2 GENE; CAUSAL ATTRIBUTION; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; HEART VENTRICLE FIBRILLATION; HUMAN; IDIOPATHIC VENTRICULAR FIBRILLATION; MISSENSE MUTATION; NOTE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SUDDEN CARDIAC DEATH; WHOLE EXOME SEQUENCING; BRUGADA SYNDROME; CALCIUM SIGNALING; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; EDITORIAL; GENE IDENTIFICATION; GENETIC ANALYSIS; HEART MUSCLE CONTRACTILITY; LONG QT SYNDROME; OVERALL SURVIVAL; QT PROLONGATION;

CALMODULIN;

CALMODULIN; GENETICS; IDIOPATHIC VENTRICULAR FIBRILLATION; VENTRICULAR ARRHYTHMIA; WHOLE EXOME SEQUENCING;

CALMODULIN; DNA; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MONOMERIC CLATHRIN ASSEMBLY PROTEINS; MUTATION; VENTRICULAR FIBRILLATION;

EID: 84892756617     PISSN: 07351097     EISSN: 15583597     Source Type: Journal    
DOI: 10.1016/j.jacc.2013.07.089     Document Type: Editorial

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