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Specific phenotypes caused by RYR2 mutations relate with bradycardia but not with mutation locations in RYR2

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Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)
2 presentations
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Rare single nucleotide polymorphism of scn10a in patients with inherited primary arrhythmia syndromes

Speaker: Doctor M. Fukuyama (Otsu, JP)

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RYR2 mutations underlying in patients with short-coupled variant of torsade de pointes

Speaker: Doctor Y. Fujii (Otsu, JP)

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Poster session 6 - Genetic aspects of arrhythmias

Speakers: Doctor S. Ohno, Doctor M. Fukuyama, Doctor Y. Fujii
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ESC CONGRESS 2016

27 August - 31 August 2016

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