Ryanodine Receptor Mutations Presenting as Idiopathic Ventricular Fibrillation: A Report on Two Novel Familial Compound Mutations, c.6224T>C and c.13781A>G, With the Clinical Presentation of Idiopathic Ventricular Fibrillation

Title
Ryanodine Receptor Mutations Presenting as Idiopathic Ventricular Fibrillation: A Report on Two Novel Familial Compound Mutations, c.6224T>C and c.13781A>G, With the Clinical Presentation of Idiopathic Ventricular Fibrillation
Authors
Keywords
Catecholaminergic polymorphic ventricular tachycardia, Idiopathic ventricular fibrillation, Channelopathy, Genetics, Arrhythmia
Journal
PEDIATRIC CARDIOLOGY
Volume 35, Issue 8, Pages 1437-1441
Publisher
Springer Nature
Online
2014-06-20
DOI
10.1007/s00246-014-0950-2

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