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4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6

Spinocerebellar ataxia type 6 (SCA6) is a devastating midlife-onset autosomal dominant motor control disease with no known treatment. Using a hyper-expanded polyglutamine (84Q) knock-in mouse, we found that cerebellar Purkinje cell firing precision was degraded in heterozygous (SCA6(84Q/+)) mice at...

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Bibliografski detalji
Izdano u:Sci Rep
Glavni autori: Jayabal, Sriram, Chang, Hui Ho Vanessa, Cullen, Kathleen E., Watt, Alanna J.
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2016
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Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4933933/
https://ncbi.nlm.nih.gov/pubmed/27381005
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep29489
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