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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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| Vydáno v: | J Neurosci Res |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2016
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| Témata: | |
| On-line přístup: | 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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