RYR2 gene exon 3 deletion as a cause of convergent polymorphic catecholaminergic ventricular tachycardia and cardiomyopathy characterized by LV systolic dysfunction.

30 August 2024 (08:00 - 17:30)
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Congress Presentation Part of: Monogenetic cardiac diseases Clinical ESC Professional Premium Access ESC Congress 2024 European Society of Cardiology

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