A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence

Journal of the American College of Cardiology

Volumn 63, Issue 3, 2014, Pages 259-266

  Marsman, Roos F ^a   Barc, Julien ^a,b   Beekman, Leander ^a   Alders, Marielle ^a   Dooijes, Dennis ^c   Van Den Wijngaard, Arthur ^d   Ratbi, Ilham ^e   Sefiani, Abdelaziz ^e   Bhuiyan, Zahurul A ^a,f   Wilde, Arthur A M ^a,g   Bezzina, Connie R ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d MAASTRICHT UNIVERSITY   (Netherlands)

^e MOHAMMED V UNIVERSITY   (Morocco)

^f LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^g KING ABDULAZIZ UNIVERSITY   (Saudi Arabia)

Author keywords

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

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CALMODULIN;

ADOLESCENT; ADULT; ARTICLE; ASYMPTOMATIC DISEASE; CALM1 GENE; CHILD; CLINICAL ARTICLE; EXOME; FAMILY; FEMALE; GENE MUTATION; GENE SEQUENCE; HEART VENTRICLE FIBRILLATION; HUMAN; IDIOPATHIC VENTRICULAR FIBRILLATION; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR; MALE; MIDDLE AGED; MISSENSE MUTATION; OUT OF HOSPITAL CARDIAC ARREST; PRIORITY JOURNAL; QT PROLONGATION; RESUSCITATION; SCHOOL CHILD; SIBLING; SUDDEN DEATH; YOUNG ADULT; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CONTROLLED STUDY; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; GENE; GENE IDENTIFICATION; GENE MAPPING; GENETIC ANALYSIS; GENETIC CODE; GENETIC HETEROGENEITY; GENETIC VARIABILITY; HETEROZYGOSITY; HOMOZYGOSITY; LONG QT SYNDROME; SINGLE NUCLEOTIDE POLYMORPHISM; SUDDEN CARDIAC DEATH;

CALMODULIN; CAM; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CPVT; DEOXYRIBONUCLEIC ACID; DNA; ECG; ELECTROCARDIOGRAM/ELECTROCARDIOGRAPHIC; EXOME SEQUENCING; GENETICS; ICD; IDIOPATHIC VENTRICULAR FIBRILLATION; IDIOPATHIC VENTRICULAR FIBRILLATION; IMPLANTABLE CARDIOVERTER-DEFIBRILLATOR; IVF; LONG-QT SYNDROME; LQTS; OHCA; OUT-OF-HOSPITAL CARDIAC ARREST; VENTRICULAR ARRHYTHMIA;

ADOLESCENT; CALMODULIN; CHILD; DNA; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MONOMERIC CLATHRIN ASSEMBLY PROTEINS; MUTATION; PEDIGREE; VENTRICULAR FIBRILLATION;

EID: 84892407727     PISSN: 07351097     EISSN: 15583597     Source Type: Journal    
DOI: 10.1016/j.jacc.2013.07.091     Document Type: Article

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