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Role of common variants and new genes associated with arrhythmogenic cardiomyopathy

30 August 2024 (08:00 - 17:30)
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Congress Presentation Part of: Novel mechanisms of arrhythmogenic cardiac disease Genetics, Epigenetics, ncRNA ESC Professional Premium Access ESC Congress 2024 European Society of Cardiology

About the speaker

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Doctor Julien barc

Institute of Thorax, Nantes (France)

5 More presentations in this session

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Serum exosomal long non-coding RNA H19 as a theragnostic target for atrial fibrillation
Ms J. Kang (Seoul, KR)
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The CNP analogue vosoritide reduces arrhythmia in diabetic cardiomyopathy via cGMP-dependent PDE2 stimulation on cellular and organ level
Ms R. Firneburg (Dresden, DE)
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Investigating the role of an orphan nuclear receptor NR4A1 in atrial fibrillation
Mr C. Yiu (Oxford, GB)
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Characterization of knock-in zebrafish models with a novel SLC4A3 variant identified in a short QT syndrome family
Ms M. Zhu (Suita, JP)
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The H222P-Lamin mutation induces heart failure via impaired mitochondrial calcium uptake in human cardiac laminopathy
Professor J. Hulot (Paris, FR)
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Novel mechanisms of arrhythmogenic cardiac disease
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The Event

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ESC Congress 2024

30 August - 2 September 2024

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources