Genetic Diversity of SCN5A Gene and Its Possible Association with the Concealed Form of Brugada Syndrome Development in Polish Group of Patients

Brugada Syndrome (BS) is an inherited channelopathy associated with a high incidence of sudden cardiac death. The paper presents the discovery of new genetic variants of SCN5A gene which might be associated with the development of a concealed form of Brugada Syndrome. The study involved a group of 5...

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Detalles Bibliográficos
Autores principales: Uziębło-Życzkowska, Beata, Gielerak, Grzegorz, Siedlecki, Paweł, Pająk, Beata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220633/
https://www.ncbi.nlm.nih.gov/pubmed/25401102
http://dx.doi.org/10.1155/2014/462609

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220633/
https://www.ncbi.nlm.nih.gov/pubmed/25401102
http://dx.doi.org/10.1155/2014/462609

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