Primary electrical disorder or primary cardiomyopathy?: A case with a unique association of noncompaction cardiomyopathy and cathecolaminergic polymorphic ventricular tachycardia caused by ryanodine receptor mutation

2013-03-12

Circulation (Baltimore) , Volume 127 - Issue 10 p. 1165- 1166

Additional Metadata
Keywords	Holter monitoring, adult, angiocardiography, case report, catecholaminergic polymorphic ventricular tachycardia, clinical feature, defibrillator, disease association, drug dose titration, dyspnea, electrocardiography, faintness, fatigue, female, gene mutation, heart left ventricle outflow tract, heart palpitation, heart repolarization, human, note, nuclear magnetic resonance imaging, optimal drug dose, priority journal, sinus bradycardia, ventricular noncompaction
Persistent URL	doi.org/10.1161/CIRCULATIONAHA.112.144949, hdl.handle.net/1765/39549
Journal	Circulation (Baltimore)
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Szentpáli, Z., Szili-Török, T., & Caliskan, K. (2013). Primary electrical disorder or primary cardiomyopathy?: A case with a unique association of noncompaction cardiomyopathy and cathecolaminergic polymorphic ventricular tachycardia caused by ryanodine receptor mutation. Circulation (Baltimore) (Vol. 127, pp. 1165–1166). doi:10.1161/CIRCULATIONAHA.112.144949

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