Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

BACKGROUND: Phenotypic overlap of type 3 long QT syndrome (LQT3), Brugada syndrome (BrS), cardiac conduction disease (CCD), and sinus node dysfunction (SND) is observed with SCN5A mutations. SCN5A‐E1784K is the most common mutation associated with BrS and LQTS3. The present study examines the genoty...

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Detalles Bibliográficos
Autores principales: Veltmann, Christian, Barajas‐Martinez, Hector, Wolpert, Christian, Borggrefe, Martin, Schimpf, Rainer, Pfeiffer, Ryan, Cáceres, Gabriel, Burashnikov, Elena, Antzelevitch, Charles, Hu, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015375/
https://www.ncbi.nlm.nih.gov/pubmed/27381756
http://dx.doi.org/10.1161/JAHA.116.003379

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015375/
https://www.ncbi.nlm.nih.gov/pubmed/27381756
http://dx.doi.org/10.1161/JAHA.116.003379

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