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Donepezil increases resistance to induced seizures in a mouse model of Dravet syndrome
De novo loss‐of‐function mutations in SCN1A are the main cause of Dravet syndrome, a catastrophic encephalopathy characterized by recurrent early‐life febrile seizures, a number of other afebrile seizure types that are often refractory to treatment, and behavioral abnormalities including social defi...
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| Publicado en: | Ann Clin Transl Neurol |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6689688/ https://ncbi.nlm.nih.gov/pubmed/31402621 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50848 |
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