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The SCN5A point mutation M1875T, associated with familial atrial fibrillation, causes a gain-of-function effect of the cardiac Nav1.5 channel in atrial cardiomyocytes

23 April 2021 (16:00 - 22:20)
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Congress Presentation Part of: Oral abstract session - WGCCE Arrhythmias EHRA Premium Access EHRA 2021

About the speaker

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Doctor Molly O'Reilly

Amsterdam University Medical Centre (AUMC), Amsterdam (Netherlands (The))

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Desmosomal vulnerability renders left atria more susceptible to detrimental effects of androgenic anabolic steroids
Ms L. Sommerfeld (Hamburg, DE)
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CaMKII as a therapeutic target in catecholaminergic polymorphic ventricular tachycardia type 1
Mr M. Sadredini (Oslo, NO)
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OPN5 a new optogenetic receptor to study Gq signalling in the heart with light
Mr A. Wagdi Mohamed (Goettingen, DE)
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Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1
Doctor O. Svecova (Brno, CZ)
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When multiple caveolins make the difference: Cav1 partly compensates Cav3 alterations and rescues ion channels expression.
Doctor P. Benzoni (Milan, IT)
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Access the full session

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Oral abstract session - WGCCE

The Event

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EHRA 2021

23 April 2021 16:00 CET
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