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Altered Kv3.3 channel gating in early-onset spinocerebellar ataxia type 13
Mutations in Kv3.3 cause spinocerebellar ataxia type 13 (SCA13). Depending on the causative mutation, SCA13 is either a neurodevelopmental disorder that is evident in infancy or a progressive neurodegenerative disease that emerges during adulthood. Previous studies did not clarify the relationship b...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3413486/ https://ncbi.nlm.nih.gov/pubmed/22289912 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2012.228205 |
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