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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...
Shranjeno v:
| izdano v: | Dis Model Mech |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Company of Biologists Ltd
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6906634/ https://ncbi.nlm.nih.gov/pubmed/31704708 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.040840 |
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