ESC Premium Access

Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia

Topic: Genetic aspects of arrhythmias

Congress Presentation

About the speaker

Doctor Koichiro Takayama

National Cerebral & Cardiovascular Center, Suita (Japan)
0 follower

9 more presentations in this session

Atrial fibrillation in long QT syndrome as a risk indicator of cardiac events

Speaker: Professor P. Platonov (Lund, SE)

Thumbnail

Identification of TNFSF13, SPATC1L, SLC22A25, and SALL4 as novel susceptibility loci for atrial fibrillation in Japanese individuals by an exome-wide association study

Speaker: Doctor H. Horibe (Tajimi, JP)

Thumbnail

Genetic background of sudden cardiac death caused by idiopathic myocardial fibrosis.

Speaker: Mr L. Holmstrom (Oulu, FI)

Thumbnail

Gene-based risk stratification for cardiac disorders in LMNA mutation carriers

Speaker: Doctor S. Nishiuchi (Tenri, JP)

Thumbnail

Unexpected risk profile in a large paediatric population with Brugada syndrome.

Speaker: Doctor A. Mazzanti (Pavia, IT)

Thumbnail

Access the full session

Genetics and cardiac arrhythmias

Speakers: Doctor K. Takayama, Professor P. Platonov, Doctor H. Horibe, Mr L. Holmstrom, Doctor S. Nishiuchi...
Thumbnail

About the event

Image

ESC Congress 2017

26 August - 30 August 2017

Sessions Presentations