In vivo cerebellar circuit function is disrupted in an mdx mouse model of Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is a debilitating and ultimately lethal disease involving progressive muscle degeneration and neurological dysfunction. DMD is caused by mutations in the dystrophin gene, which result in extremely low or total loss of dystrophin protein expression. In the brain, dys...

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Detalles Bibliográficos
Autores principales: Stay, Trace L., Miterko, Lauren N., Arancillo, Marife, Lin, Tao, Sillitoe, Roy V.
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/PMC6906634/
https://www.ncbi.nlm.nih.gov/pubmed/31704708
http://dx.doi.org/10.1242/dmm.040840

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906634/
https://www.ncbi.nlm.nih.gov/pubmed/31704708
http://dx.doi.org/10.1242/dmm.040840

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