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Cellular and circuit mechanisms underlying spinocerebellar ataxias
Degenerative ataxias are a common form of neurodegenerative disease that affect about 20 individuals per 100,000. The autosomal dominant spinocerebellar ataxias (SCAs) are caused by a variety of protein coding mutations (single nucleotide changes, deletions and expansions) in single genes. Affected...
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| Foilsithe in: | J Physiol |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
John Wiley and Sons Inc.
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4983629/ https://ncbi.nlm.nih.gov/pubmed/27198167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/JP271897 |
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