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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...
Guardat en:
| Publicat a: | Ann Clin Transl Neurol |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2019
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| Matèries: | |
| Accés en línia: | 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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