Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy
Abstract Spinocerebellar ataxia type 2 (SCA2) is an incurable and genetic neurodegenerative disorder. The disease is characterized by progressive degeneration of several brain regions, resulting in severe motor and non-motor clinical manifestations. The mutation causing SCA2 disease is an abnormal e...
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| Auteurs principaux: | , , , , , , , , , , , , |
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| Format: | article |
| Langue: | EN |
| Publié: |
Nature Publishing Group
2021
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| Sujets: | |
| Accès en ligne: | https://doaj.org/article/b63aca6d2a754206b576ac751ce40616 |
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