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Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1

Session: Ion channel (dys)function
Topic: Basic Science
Speaker: Doctor O. Svecova (Brno, CZ)
Event: EHRA 2021

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Doctor Olga Svecova

Masaryk University, Brno (Czechia)
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5 more presentations in this session

Orai1 Ca2+ channel: new actor involved in left ventricular hypertrophy

Speaker: Assistant Professor J. Sabourin (Chatenay-Malabry, FR)

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Nocturnal Bradycardia: Revisiting a 90 year old theory

Speaker: Doctor A. D'souza (London, GB)

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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

Speaker: Doctor M. O'Reilly (Amsterdam, NL)

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Piezo1 and BKCa channels in human atrial fibroblasts: interplay and remodelling in atrial fibrillation

Speaker: Doctor R. Peyronnet (Freiburg, DE)

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Ion channel (dys)function - discussion

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Access the full session

Ion channel (dys)function

Speakers: Doctor O. Svecova, Assistant Professor J. Sabourin, Doctor A. D'souza, Doctor M. O'Reilly, Doctor R. Peyronnet
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EHRA 2021

23 April - 25 April 2021

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