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Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregation
Spinocerebellar ataxia type 14 (SCA14) is a subtype of the autosomal dominant cerebellar ataxias that is characterized by slowly progressive cerebellar dysfunction and neurodegeneration. SCA14 is caused by mutations in the PRKCG gene, encoding protein kinase C gamma (PKCγ). Despite the identificatio...
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| 出版年: | Acta Neuropathol Commun |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6151931/ https://ncbi.nlm.nih.gov/pubmed/30249303 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-018-0600-7 |
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