Novel trans-2,3-enoyl-CoA reductase–like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3

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Elsevier Inc.

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Cpvt, Inherited channelopathy, Long qt syndrome, Sudden cardiac death, Tecrl, Flecainide, Nadolol, Oxidoreductase, Propranolol, Trans 2,3 enoyl coa reductase, Unclassified drug, Adolescent, Article, Cardiovascular magnetic resonance, Case report, Catecholaminergic polymorphic ventricular tachycardia, Child, Clinical article, Clinical feature, Disease association, Dizziness, Echocardiography, Electrical storm (heart), Electrophysiology, Exercise test, Family history, Female, Follow up, Frameshift mutation, Genetic variation, Heart palpitation, Heart ventricle extrasystole, Heart ventricle function, Heterozygosity, Holter monitoring, Homozygosity, Human, Low drug dose, Medication compliance, Mitral valve prolapse, Mitral valve regurgitation, Nausea, Physiological stress, Preschool child, Primary prevention, Qt prolongation, School child, Sport, T wave, Whole exome sequencing

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