ESC 365 - Genetic variation rs6795970 of the SCN10A gene is associated with PR interval in young population of Republic of Moldova

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

Session: Inherited cardiac disorders

Topic: Ion Channel Disorders

Speaker: Mrs C. Butovscaia (Chisinau, MD)

Event: ESC Congress 2022

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About the speaker

Mrs Cristina Butovscaia

State University of Medicine and Pharmacy, Chisinau (Moldova (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)

Functional analysis of novel SCN5A mutations related to Brugada syndrome

Speaker: Mrs H. Namgoong (Seoul, KR)

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

About the event

ESC Congress 2022

26 August - 29 August 2022

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