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Vulnerability of Human Cerebellar Neurons to Degeneration in Ataxia-Causing Channelopathies
Mutations in ion channel genes underlie a number of human neurological diseases. Historically, human mutations in ion channel genes, the so-called channelopathies, have been identified to cause episodic disorders. In the last decade, however, mutations in ion channel genes have been demonstrated to...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219590/ https://www.ncbi.nlm.nih.gov/pubmed/35757096 http://dx.doi.org/10.3389/fnsys.2022.908569 |