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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Publicat a:Eur Heart J
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2019
Matèries:
Basic Science
Accés en línia: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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