Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome

por Zaklyazminskaya, Elena, Shestak, Anna, Podolyak, Dmitry, Komoliatova, Vera, Makarov, Leonid, Novitskaya, Anna, Revishvili, Amiran
Publicado 2022

Coexistence of Two Rare Genetic Variants in Canonical and Non-canonical Exons of SCN5A: A Potential Source of Misinterpretation

por Shestak, Anna G., Makarov, Leonid M., Komoliatova, Vera N., Kolesnikova, Irina V., Skorodumova, Liubov O., Generozov, Edward V., Zaklyazminskaya, Elena V.
Publicado 2021

Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome

por Zaklyazminskaya, Elena, Polyak, Margarita, Shestak, Anna, Sadekova, Mariam, Komoliatova, Vera, Kiseleva, Irina, Makarov, Leonid, Podolyak, Dmitriy, Glukhov, Grigory, Zhang, Han, Abramochkin, Denis, Sokolova, Olga S.
Publicado 2022