Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference14 articles.
1. Genotype- and phenotype-guided management of congenital long QT syndrome;Giudicessi;Curr Probl Cardiol,2013
2. Cardiovascular magnetic resonance in myocarditis: a JACC White Paper;Friedrich;J Am Coll Cardiol,2009
3. SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism;McNair;J Am Coll Cardiol,2011
4. Long QT syndrome and dilated cardiomyopathy with SCN5A p.R1193Q polymorphism: cardioverter-defibrillator implantation at 27 months;Kwon;Pacing Clin Electrophysiol,2012
5. The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden death;Shi;Europace,2008
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