Motor axonopathies in a mouse model of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease caused by deleterious mutations in the DMD gene which encodes the dystrophin protein. Skeletal muscle weakness and eventual muscle degradation due to loss of dystrophin are well-documented pathological hallmarks of DMD. In contrast,...

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Detalles Bibliográficos
Autores principales: Dhindsa, Justin S., McCall, Angela L., Strickland, Laura M., Fusco, Anna F., Kahn, Amanda F., ElMallah, Mai K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265344/
https://www.ncbi.nlm.nih.gov/pubmed/32488044
http://dx.doi.org/10.1038/s41598-020-65824-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265344/
https://www.ncbi.nlm.nih.gov/pubmed/32488044
http://dx.doi.org/10.1038/s41598-020-65824-1

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