Dilated Cardiomyopathy Phenotype-Associated Left Ventricular Noncompaction and Congenital Long QT Syndrome Type-2 in Infants With KCNH2 Gene Mutation: Anesthetic Considerations
Author:
Publisher
Elsevier BV
Subject
Anesthesiology and Pain Medicine,Cardiology and Cardiovascular Medicine
Reference30 articles.
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3. Familial long QT syndrome and late development of dilated cardiomyopathy in a child with a KCNQ1 mutation: A case report;Allen;Heart Rhythm Case Rep,2015
4. Long QT syndrome and dilated cardiomyopathy with SCN5A p.R1193Q polymorphism: Cardioverter-defibrillator implantation at 27 months;Kwon;Pacing Clin Electrophysiol,2012
5. SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism;McNair;J Am Coll Cardiol,2011
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