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Epilepsy channelopathies go neddy: stabilizing Na(V)1.1 channels by neddylation
Loss-of-function mutations of SCN1A encoding the pore-forming α subunit of the Na(V)1.1 neuronal sodium channel cause a severe developmental epileptic encephalopathy, Dravet syndrome (DS). In this issue of the JCI, Chen, Luo, Gao, et al. describe a phenocopy for DS in mice deficient for posttranslat...
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| Publicado no: | J Clin Invest |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8262487/ https://ncbi.nlm.nih.gov/pubmed/33855971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI148370 |
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