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Doctor Megumi Fukuyama

Shiga University of Medical Science, Otsu (Japan)
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Calmodulinopathy is a common cause of critical cardiac phenotypes in fetus and infancy
Presentation
Calmodulinopathy is a common cause of critical cardiac phenotypes in fetus and infancy
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Novel RYR2 mutations causative for long QT syndromes
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Novel RYR2 mutations causative for long QT syndromes
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Rare single nucleotide polymorphism of scn10a in patients with inherited primary arrhythmia syndromes
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Rare single nucleotide polymorphism of scn10a in patients with inherited primary arrhythmia syndromes
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