Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

Mutations affecting ryanodine receptor (RyR) calcium release channels commonly underlie congenital myopathies. Although these channels are known principally for their essential roles in muscle contractility, mutations in the human RYR1 gene result in a broad spectrum of phenotypes, including muscle...

Descripción completa

Detalles Bibliográficos
Autores principales: Chagovetz, Alexis A., Klatt Shaw, Dana, Ritchie, Erin, Hoshijima, Kazuyuki, Grunwald, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906632/
https://www.ncbi.nlm.nih.gov/pubmed/31383689
http://dx.doi.org/10.1242/dmm.038844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906632/
https://www.ncbi.nlm.nih.gov/pubmed/31383689
http://dx.doi.org/10.1242/dmm.038844

Ejemplares similares