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Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7
Spinocerebellar ataxia type 7 (SCA7) is a rare autosomal dominant neurodegenerative disorder characterized by progressive neuronal loss in the cerebellum, brainstem, and retina, leading to cerebellar ataxia and blindness as major symptoms. SCA7 is due to the expansion of a CAG triplet repeat that is...
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| Pubblicato in: | Neurotherapeutics |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer International Publishing
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6985300/ https://ncbi.nlm.nih.gov/pubmed/31432449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-019-00778-5 |
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