Speaker illustration

Miss Anastasia Zaytseva

National Medical and Research Almazov Centre, Saint Petersburg (Russian Federation)

Two novel mutations in SCN5A gene cause enhanced inactivation and lead to Brugada syndrome

Event: ESC CONGRESS 2019

Topic: Arrhythmias

Session: Electrophysiology and arrhythmias


Electrophysiological characteristics of A1294G substitution in Nav1.5 channel, associated with combined clinical phenotype

Event: ESC Congress 2018

Topic: Ion Channels, Electrophysiology

Session: Ion channels - Related pathologies


Biophysical consequences of missense mutations associated with Brugada syndrome

Event: Frontiers in CardioVascular Biology 2018

Topic: Ion Channels, Electrophysiology

Session: Basic Science - Cardiac Biology and Physiology


This platform is supported by

logo Novo Nordisk