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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Bibliografische gegevens
Gepubliceerd in:Sci Rep
Hoofdauteurs: Dhindsa, Justin S., McCall, Angela L., Strickland, Laura M., Fusco, Anna F., Kahn, Amanda F., ElMallah, Mai K.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group UK 2020
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7265344/
https://ncbi.nlm.nih.gov/pubmed/32488044
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-65824-1
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