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Presentations

Contribution of clinically relevant copy number variations in long QT syndrome: a large cohort study

Event: EHRA 2024

Topic: Genetic Aspects of Arrhythmias

Session: Basic science: genetic

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FHOD3 is a novel disease causing gene in hypertrophic cardiomyopathy

Event: ESC Congress 2018

Topic: Hypertrophic Cardiomyopathy

Session: Genetics in cardiomyopathies

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