ESC 365 - RYR2 gene exon 3 deletion as a cause of convergent polymorphic catecholaminergic ventricular tachycardia and cardiomyopathy characterized by LV systolic dysfunction.

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

Session: Monogenetic cardiac diseases

Topic: Clinical

Speaker: Doctor J. Segura-Aumente (Jaen, ES)

Event: ESC Congress 2024

Congress Presentation

About the speaker

Doctor Jose Maria Segura-Aumente

General Hospital of H.U. of Jaen, Jaen (Spain)

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Monogenetic cardiac diseases

Speakers: Doctor J. Segura-Aumente, Professor C. van Duijn, Doctor J. Tomlinson, Professor E. Tham

About the event

ESC Congress 2024

30 August - 2 September 2024

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