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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...

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Detalhes bibliográficos
Main Authors: Mock, Allan F, Richardson, Jessica L, Hsieh, Jui-Yi, Rinetti, Gina, Papazian, Diane M
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2933717/
https://ncbi.nlm.nih.gov/pubmed/20712895
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2202-11-99
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