Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome

BACKGROUND: Inherited loss of function mutations in SCN5A have been linked to overlapping syndromes including cardiac conduction disease and Brugada syndrome (BrS). The mechanisms responsible for the development of one without the other are poorly understood. METHODS: Direct sequencing was performed...

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Detalhes bibliográficos
Main Authors: Hu, Dan, Barajas-Martinez, Hector, Nesterenko, Vladislav V., Pfeiffer, Ryan, Guerchicoff, Alejandra, Cordeiro, Jonathan M., Curtis, Anne B., Pollevick, Guido D., Wu, Yuesheng, Burashnikov, Elena, Antzelevitch, Charles
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2916871/
https://ncbi.nlm.nih.gov/pubmed/20025708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1540-8159.2009.02642.x
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