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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...
Autores principales: | Stay, Trace L., Miterko, Lauren N., Arancillo, Marife, Lin, Tao, Sillitoe, Roy V. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
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 |
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