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Altered brain state during episodic dystonia in tottering mice decouples primary motor cortex from limb kinematics
Episodic Ataxia Type 2 (EA2) is a rare neurological disorder caused by a mutation in the CACNA1A gene, encoding the P/Q-type voltage-gated Ca(2+) channel important for neurotransmitter release. Patients with this channelopathy exhibit both cerebellar and cerebral pathologies, suggesting the conditio...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554815/ https://www.ncbi.nlm.nih.gov/pubmed/37800168 http://dx.doi.org/10.3389/dyst.2023.10974 |