Loss of dysferlin or myoferlin results in differential defects in excitation–contraction coupling in mouse skeletal muscle

Muscular dystrophies are disorders characterized by progressive muscle loss and weakness that are both genotypically and phenotypically heterogenous. Progression of muscle disease arises from impaired regeneration, plasma membrane instability, defective membrane repair, and calcium mishandling. The...

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Detalles Bibliográficos
Autores principales: Barefield, David Y., Sell, Jordan J., Tahtah, Ibrahim, Kearns, Samuel D., McNally, Elizabeth M., Demonbreun, Alexis R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342512/
https://www.ncbi.nlm.nih.gov/pubmed/34354129
http://dx.doi.org/10.1038/s41598-021-95378-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342512/
https://www.ncbi.nlm.nih.gov/pubmed/34354129
http://dx.doi.org/10.1038/s41598-021-95378-9

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