ESC 365 - Functional analysis of novel SCN5A mutations related to Brugada syndrome

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Functional analysis of novel SCN5A mutations related to Brugada syndrome

Session: Inherited cardiac disorders

Topic: Ion Channel Disorders

Speaker: Mrs H. Namgoong (Seoul, KR)

Event: ESC Congress 2022

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Mrs Hyun Namgoong

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

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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 (Monzino, 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)

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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

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