Back

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

27 August 2017 (11:09 - 11:18)
Organised by:
Congress Presentation Part of: Genetics and cardiac arrhythmias Genetic aspects of arrhythmias ESC Premium Access ESC Congress 2017

About the speaker

Photo
Doctor Hideki Horibe

Gifu Prefectural Tajimi Hospital, Tajimi (Japan)

9 More presentations in this session

Presentation thumbnail
Atrial fibrillation in long QT syndrome as a risk indicator of cardiac events
Professor P. Platonov (Lund, SE)
Abstract Slides Video
Presentation thumbnail
Genetic background of sudden cardiac death caused by idiopathic myocardial fibrosis.
Mr L. Holmstrom (Oulu, FI)
Abstract Slides Video
Presentation thumbnail
Gene-based risk stratification for cardiac disorders in LMNA mutation carriers
Doctor S. Nishiuchi (Tenri, JP)
Abstract Slides Video
Presentation thumbnail
Unexpected risk profile in a large paediatric population with Brugada syndrome.
Doctor A. Mazzanti (Pavia, IT)
Abstract
Presentation thumbnail
Desmoglein 2 gene mutation (DSG2-F531C) caused arrhythmogenic right ventricular cardiomyopathy in human and mice is gene dose-dependent
Doctor D. Wang (Nanjing, CN)
Abstract

Access the full session

Session thumbnail
Genetics and cardiac arrhythmias

The Event

Event poster

ESC Congress 2017

27 August 2017 11:09 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources