Speaker illustration

Doctor Megumi Fukuyama

Shiga University of Medical Science, Otsu (Japan)

Calmodulinopathy is a common cause of critical cardiac phenotypes in fetus and infancy

Event: ESC Congress 2022

Topic: Ion Channel Disorders

Session: Emerging role of genetic testing for ventricular arrhythmia management

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Novel RYR2 mutations causative for long QT syndromes

Event: ESC CONGRESS 2017

Topic: Genetic aspects of arrhythmias

Session: Genetic basis

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Rare single nucleotide polymorphism of scn10a in patients with inherited primary arrhythmia syndromes

Event: ESC CONGRESS 2016

Topic: Genetic aspects of arrhythmias

Session: Genetic aspects of arrhythmias

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