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Calmodulin (CaM) mutations are associated with cardiac arrhythmia susceptibility including congenital long QT syndrome (LQTS).The purpose of this study was to determine the clinical, genetic, and functional features of 2 novel CaM mutations in children with life-threatening ventricular arrhythmias.The clinical and genetic features of 2 congenital arrhythmia cases associated with 2 novel CaM gene mutations...
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