The expression of the rare caveolin-3 variant T78M alters cardiac ion channels function and membrane excitability

AIMS: Caveolinopathies are a family of genetic disorders arising from alterations of the caveolin-3 (cav-3) gene. The T78M cav-3 variant has been associated with both skeletal and cardiac muscle pathologies but its functional contribution, especially to cardiac diseases, is still controversial. Here...

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Detalles Bibliográficos
Autores principales: Campostrini, Giulia, Bonzanni, Mattia, Lissoni, Alessio, Bazzini, Claudia, Milanesi, Raffaella, Vezzoli, Elena, Francolini, Maura, Baruscotti, Mirko, Bucchi, Annalisa, Rivolta, Ilaria, Fantini, Matteo, Severi, Stefano, Cappato, Riccardo, Crotti, Lia, J. Schwartz, Peter, DiFrancesco, Dario, Barbuti, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852518/
https://www.ncbi.nlm.nih.gov/pubmed/28898996
http://dx.doi.org/10.1093/cvr/cvx122

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