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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Pubblicato in:Eur Heart J
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2019
Soggetti:
Basic Science
Accesso online: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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