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Purkinje cell

  • RESEARCH ARTICLE
    In vivo cerebellar circuit function is disrupted in an mdx mouse model of Duchenne muscular dystrophy
    Trace L. Stay, Lauren N. Miterko, Marife Arancillo, Tao Lin, Roy V. Sillitoe
    Disease Models & Mechanisms 2020 13: dmm040840 doi: 10.1242/dmm.040840 Published 9 December 2019

    Summary: The mdx mouse model of Duchenne muscular dystrophy (DMD) has in vivo abnormalities in cerebellar spike firing, which could contribute to the neurological symptoms observed in individuals with DMD.

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