Prevalence of significant genetic variants in congenital long QT syndrome genes is largely underestimated

by Elena V. Zaklyazminskaya, Hugues eAbriel
Published 2012-04-01

New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling

by Margarita E. Polyak, Elena V. Zaklyazminskaya
Published 2020-04-01

Editorial: Inherited Arrhythmias of the Cardiac Sodium Channel Nav1.5

by Mohamed-Yassine Amarouch, Elena V. Zaklyazminskaya, Jean-Sébastien Rougier
Published 2021-08-01

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels

by Anna G. Shestak, Anna A. Bukaeva, Siamak Saber, Elena V. Zaklyazminskaya
Published 2021-02-01

Mixed Hypertrophic and Dilated Phenotype of Cardiomyopathy in a Patient With Homozygous In-Frame Deletion in the MyBPC3 Gene Treated as Myocarditis for a Long Time

by Olga Blagova, Indira Alieva, Eugenia Kogan, Alexander Zaytsev, Vsevolod Sedov, S. Chernyavskiy, Yulia Surikova, Ilya Kotov, Elena V. Zaklyazminskaya
Published 2020-09-01

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

by Anna G. Shestak, Leonid M. Makarov, Vera N. Komoliatova, Irina V. Kolesnikova, Liubov O. Skorodumova, Edward V. Generozov, Elena V. Zaklyazminskaya
Published 2021-09-01