Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome

Genetic variants in SCN5A gene were identified in patients with various arrhythmogenic conditions including Brugada syndrome. Despite significant progress of last decades in studying the molecular mechanism of arrhythmia-associated SCN5A mutations, the understanding of relationship between genetics,...

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Detalles Bibliográficos
Autores principales: Zaytseva, Anastasia K., Kiselev, Artem M., Boitsov, Alexander S., Fomicheva, Yulia V., Pavlov, Georgii S., Zhorov, Boris S., Kostareva, Anna A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920867/
https://www.ncbi.nlm.nih.gov/pubmed/35300108
http://dx.doi.org/10.1016/j.bbrep.2022.101249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920867/
https://www.ncbi.nlm.nih.gov/pubmed/35300108
http://dx.doi.org/10.1016/j.bbrep.2022.101249

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