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 (00:00 - 00:00)
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Congress Presentation Part of: Oral abstract session - WGCCE Arrhythmias EHRA Premium Access EHRA 2021

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