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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Eur Heart J
Main Authors: 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
Idioma:Inglês
Publicado em: Oxford University Press 2019
Assuntos:
Basic Science
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados