ESC Professional Premium Access

Functional analysis of novel SCN5A mutations related to Brugada syndrome

Topic: Ion Channel Disorders

Congress Presentation

About the speaker

Mrs Hyun Namgoong

Seoul National University College of Medicine, Seoul (Korea (Republic of))
0 follower

4 more presentations in this session

Clinical role of genetic testing for overlapping between Brugada syndrome and arrhythmogenic right ventricular cardiomyopathy

Speaker: Assistant Professor J. Jeong (Seoul, KR)


Reinterpretation of variant of unknown significance in the clinical setting of inherited cardiac conditions

Speaker: Doctor V. Novelli (Milan, IT)


Genetic variation rs6795970 of the SCN10A gene is associated with PR interval in young population of Republic of Moldova

Speaker: Mrs C. Butovscaia (Chisinau, MD)


Risk stratification of sudden cardiac death in subjects with asymptomatic ventricular preexcitation: diagnostic value of non-invasive and invasive methods

Speaker: Doctor L. Pilon Kaial (Rosario, AR)


Access the full session

Inherited cardiac disorders

Speakers: Mrs H. Namgoong, Assistant Professor J. Jeong, Doctor V. Novelli, Mrs C. Butovscaia, Doctor L. Pilon Kaial

About the event


ESC Congress 2022

26 August - 29 August 2022

Sessions Presentations

ESC 365 is supported by

logo Novo Nordisk
logo Bristol Myers Squibb