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A mutation in the gene encoding the tbx5 transcription factor is associated with the Brugada Syndrome

29 August 2017 (15:35 - 16:25)
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Congress Presentation Part of: Cellular and molecular electrophysiology Ion channels and electrophysiology ESC Premium Access ESC Congress 2017

About the speaker

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Professor Ricardo Caballero

Complutense University of Madrid, Madrid (Spain)

6 More presentations in this session

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Characterization of a novel genetic variant associated with Brugada syndrome: beta-2-syntrophin mutation impairs interaction with SCN5A and reduces Na+ current in human cardiomyocytes
Doctor C. Schmidt (Goettingen, DE)
Abstract
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Optogenetic cardioversion terminates atrial fibrillation in wild-type mice after gene transfer
Doctor T. Beiert (Bonn, DE)
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Local epicardial light pulse terminates ventricular arrhythmias in the adult rat heart upon optogenetic modification: towards biological shockless defibrillation.
Mr E. Nyns (Rotterdam, NL)
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Patient-specific iPSC-derived cardiomyocytes reveal a disease-causing role of an ACTN2 mutation in HCM and an unexpected LQT phenotype
Doctor M. Lemoine (Hamburg, DE)
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Structural and functional plasticity of myocardial slices in response to prolonged mechanical loading and unloading in vitro
Mr S. Watson (London, GB)
Abstract Slides

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Cellular and molecular electrophysiology

The Event

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ESC Congress 2017

29 August 2017 15:35 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources