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Cardiac phenotype and prognosis of patients with mutations in NKX2.5 gene

28 August 2016 (09:15 - 09:24)
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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 Philippe Maury

Rangueil Hospital of Toulouse, Toulouse (France)

9 More presentations in this session

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Whole exome sequencing of families with atrial fibrillation - a Danish nationwide study.
Doctor L. Refsgaard (Copenhagen, DK)
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Age and gender related differences in corrected QT interval in children and adolescents with LQT1 and LQT2
Doctor S. Vink (Amsterdam, NL)
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Genetic determinants of arrhythmia in dilated cardiomyopathy
Doctor U. Tayal (London, GB)
Abstract
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Location of SCN5A mutation determines severity of phenotype and response to sodium channel blockage
Mr Y. Reckman (Zwolle, NL)
Abstract Slides Video
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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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Access the full session

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Gene and arrhythmias

The Event

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ESC Congress 2016

28 August 2016 09:15 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources