טוען...
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...
שמור ב:
| הוצא לאור ב: | Dis Model Mech |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
The Company of Biologists Ltd
2019
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| נושאים: | |
| גישה מקוונת: | 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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