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

Congress Presentation

About the speaker

Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)
2 presentations
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2 more presentations in this session

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

Speaker: Doctor M. Fukuyama (Otsu, JP)


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

Speaker: Doctor Y. Fujii (Otsu, JP)


Access the full session

Poster session 6 - Genetic aspects of arrhythmias

Speakers: Doctor S. Ohno, Doctor M. Fukuyama, Doctor Y. Fujii

About the event


ESC Congress 2016

27 August - 31 August 2016

Sessions Presentations

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