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Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia

27 August 2017 (12:21 - 12:30)
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Congress Presentation Part of: Genetics and cardiac arrhythmias Genetic aspects of arrhythmias ESC Premium Access ESC Congress 2017

About the speaker

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Doctor Koichiro Takayama

National Cerebral & Cardiovascular Center, Suita (Japan)

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Atrial fibrillation in long QT syndrome as a risk indicator of cardiac events
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Identification of TNFSF13, SPATC1L, SLC22A25, and SALL4 as novel susceptibility loci for atrial fibrillation in Japanese individuals by an exome-wide association study
Doctor H. Horibe (Tajimi, JP)
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Genetic background of sudden cardiac death caused by idiopathic myocardial fibrosis.
Mr L. Holmstrom (Oulu, FI)
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Gene-based risk stratification for cardiac disorders in LMNA mutation carriers
Doctor S. Nishiuchi (Tenri, JP)
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Unexpected risk profile in a large paediatric population with Brugada syndrome.
Doctor A. Mazzanti (Pavia, IT)
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Genetics and cardiac arrhythmias

The Event

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ESC Congress 2017

27 August 2017 12:21 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources