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Genetic determinants of arrhythmia in dilated cardiomyopathy

28 August 2016 (08:48 - 08:57)
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Congress Presentation Part of: Gene and arrhythmias Genetic aspects of arrhythmias ESC Premium Access ESC Congress 2016

About the speaker

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Doctor Upasana Tayal

Imperial College London, London (United Kingdom of Great Britain & Northern Ireland)

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Location of SCN5A mutation determines severity of phenotype and response to sodium channel blockage
Mr Y. Reckman (Zwolle, NL)
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Role of implantable cardioverter defibrillator device therapy in patients with progressive Fabry disease
Mr D. Oder (Wuerzburg, DE)
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Cardiac phenotype and prognosis of patients with mutations in NKX2.5 gene
Doctor P. Maury (Toulouse, FR)
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Gene and arrhythmias

The Event

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ESC Congress 2016

28 August 2016 08:48 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources