ABCC9 is a Novel Brugada and Early Repolarization Syndrome Susceptibility Gene

BACKGROUND: Genetic defects in KCNJ8, encoding the Kir6.1 subunit of the ATP-sensitive K(+) channel (I(K-ATP)), have previously been associated with early repolarization (ERS) and Brugada (BrS) syndromes. Here we test the hypothesis genetic variants in ABCC9, encoding the ATP-binding cassette transp...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Hu, Dan, Barajas-Martínez, Hector, Terzic, Andre, Park, Sungjo, Pfeiffer, Ryan, Burashnikov, Elena, Wu, Yuesheng, Borggrefe, Martin, Veltmann, Christian, Schimpf, Rainer, Cai, John J., Nam, Gi-Byong, Deshmukh, Pramod, Scheinman, Melvin, Preminger, Mark, Steinberg, Jonathan, López-Izquierdo, Angélica, Ponce-Balbuena, Daniela, Wolpert, Christian, Haïssaguerre, Michel, Sánchez-Chapula, José Antonio, Antzelevitch, Charles
Formato: Artigo
Lenguaje:Inglês
Publicado: 2014
Materias:
Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3947869/
https://ncbi.nlm.nih.gov/pubmed/24439875
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2013.12.084
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares