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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Bibliographic Details
Published in:Dis Model Mech
Main Authors: Stay, Trace L., Miterko, Lauren N., Arancillo, Marife, Lin, Tao, Sillitoe, Roy V.
Format: Artigo
Language:Inglês
Published: The Company of Biologists Ltd 2019
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Research Article
Online Access: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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