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

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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

Session: Oral abstract session - WGCCE

Topic: Arrhythmias

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

Event: EHRA 2021

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About the speaker

Doctor Molly O'Reilly

Academic Medical Centre, Amsterdam (Netherlands (The))

2 presentations

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Oral abstract session - WGCCE

Speakers: Doctor M. O'Reilly, Ms L. Sommerfeld, Mr M. Sadredini, Mr A. Wagdi Mohamed, Doctor O. Svecova...

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EHRA 2021

23 April - 25 April 2021

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