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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

Topic: Ion channels and electrophysiology

Congress Presentation

About the speaker

Doctor Marc D Lemoine

The University Medical Center Hamburg-Eppendorf, Hamburg (Germany)
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6 more presentations in this session

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

Speaker: Doctor C. Schmidt (Heidelberg, DE)


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

Speaker: Professor R. Caballero (Madrid, ES)


Optogenetic cardioversion terminates atrial fibrillation in wild-type mice after gene transfer

Speaker: Doctor T. Beiert (Bonn, DE)


Local epicardial light pulse terminates ventricular arrhythmias in the adult rat heart upon optogenetic modification: towards biological shockless defibrillation.

Speaker: Mr E. Nyns (Leiden, NL)


Structural and functional plasticity of myocardial slices in response to prolonged mechanical loading and unloading in vitro

Speaker: Mr S. Watson (London, GB)


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Cellular and molecular electrophysiology

Speakers: Doctor M. Lemoine, Doctor C. Schmidt, Professor R. Caballero, Doctor T. Beiert, Mr E. Nyns...

About the event


ESC Congress 2017

26 August - 30 August 2017

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ESC 365 is supported by

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