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

1 September 2024 (14:35 - 14:52)
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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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