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Genetically modified rodent models of Spinocerebellar Ataxia Type 17
Spinocerebellar ataxia type 17 (SCA17) is a family member of Autosomal Dominant Cerebellar Ataxias (ADCA) characterized by variable manifestations, including cerebellar ataxia, dementia and psychiatric symptoms. Since the identification of a CAG repeat expansion in the TBP gene in a patient with ata...
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| 出版年: | J Neurosci Res |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5508981/ https://ncbi.nlm.nih.gov/pubmed/27859490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.23984 |
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