Altered Synaptic Transmission and Excitability of Cerebellar Nuclear Neurons in a Mouse Model of Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is generally regarded as a muscle-wasting disease. However, human patients and animal models of DMD also frequently display non-progressive cognitive deficits and high comorbidity with neurodevelopmental disorders, suggesting impaired central processing. Previous st...

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Detalles Bibliográficos
Autores principales: Kreko-Pierce, Tabita, Pugh, Jason R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cellular Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294606/
https://www.ncbi.nlm.nih.gov/pubmed/35865113
http://dx.doi.org/10.3389/fncel.2022.926518

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294606/
https://www.ncbi.nlm.nih.gov/pubmed/35865113
http://dx.doi.org/10.3389/fncel.2022.926518

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