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

24 April 2021 (11:35 - 11:41)
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Congress Presentation Part of: Ion channel (dys)function Basic Science EHRA Premium Access EHRA 2021

About the speaker

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Doctor Olga Svecova

Masaryk University, Brno (Czechia)

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Orai1 Ca2+ channel: new actor involved in left ventricular hypertrophy
Assistant Professor J. Sabourin (Chatenay-Malabry, FR)
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Nocturnal Bradycardia: Revisiting a 90 year old theory
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
Doctor M. O'Reilly (Amsterdam, NL)
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Piezo1 and BKCa channels in human atrial fibroblasts: interplay and remodelling in atrial fibrillation
Doctor R. Peyronnet (Freiburg, DE)
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Ion channel (dys)function - discussion

Access the full session

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Ion channel (dys)function

The Event

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EHRA 2021

24 April 2021 11:35 CET
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