ESC 365 - Specific phenotypes caused by RYR2 mutations relate with bradycardia but not with mutation locations in RYR2

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

Session: Poster session 6 - Genetic aspects of arrhythmias

Topic: Genetic aspects of arrhythmias

Speaker: Doctor S. Ohno (Suita, JP)

Event: ESC Congress 2016

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

Congress

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