RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

AIMS: The Brugada syndrome (BrS) is an inherited cardiac disorder predisposing to ventricular arrhythmias. Despite considerable efforts, its genetic basis and cellular mechanisms remain largely unknown. The objective of this study was to identify a new susceptibility gene for BrS through familial in...

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Detalles Bibliográficos
Publicado en:Eur Heart J
Autores principales: Belbachir, Nadjet, Portero, Vincent, Al Sayed, Zeina R, Gourraud, Jean-Baptiste, Dilasser, Florian, Jesel, Laurence, Guo, Hongchao, Wu, Haodi, Gaborit, Nathalie, Guilluy, Christophe, Girardeau, Aurore, Bonnaud, Stephanie, Simonet, Floriane, Karakachoff, Matilde, Pattier, Sabine, Scott, Carol, Burel, Sophie, Marionneau, Céline, Chariau, Caroline, Gaignerie, Anne, David, Laurent, Genin, Emmanuelle, Deleuze, Jean-François, Dina, Christian, Sauzeau, Vincent, Loirand, Gervaise, Baró, Isabelle, Schott, Jean-Jacques, Probst, Vincent, Wu, Joseph C, Redon, Richard, Charpentier, Flavien, Le Scouarnec, Solena
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2019
Materias:
Basic Science
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6769825/
https://ncbi.nlm.nih.gov/pubmed/31114854
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehz308
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