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Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels
BACKGROUND: The zebrafish has been suggested as a model system for studying human diseases that affect nervous system function and motor output. However, few of the ion channels that control neuronal activity in zebrafish have been characterized. Here, we have identified zebrafish orthologs of volta...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933717/ https://www.ncbi.nlm.nih.gov/pubmed/20712895 http://dx.doi.org/10.1186/1471-2202-11-99 |