Spinocerebellar Ataxia Type 7 Cerebellar Disease Requires the Coordinated Action of Mutant Ataxin-7 in Neurons and Glia, and Displays Non-Cell-Autonomous Bergmann Glia Degeneration

Spinocerebellar ataxia type 7 (SCA7) is a dominantly inherited disorder characterized by cerebellum and brainstem neurodegeneration. SCA7 is caused by a CAG/polyglutamine (polyQ) repeat expansion in the ataxin-7 gene. We previously reported that directed expression of polyQ-ataxin-7 in Bergmann glia...

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Bibliographic Details
Main Authors: Furrer, Stephanie A., Mohanachandran, Mathini S., Waldherr, Sarah M., Chang, Christopher, Damian, Vincent A., Sopher, Bryce L., Garden, Gwenn A., La Spada, Albert R.
Format: Artigo
Language:Inglês
Published: Society for Neuroscience 2011
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3256125/
https://ncbi.nlm.nih.gov/pubmed/22072678
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4000-11.2011
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