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Gene expression profiling in a mouse model of Dravet syndrome
Dravet syndrome is a severe, early-onset epileptic encephalopathy frequently resulting from de novo mutations of SCN1A. Mice with heterozygous deletion of Scn1a (Scn1a(+/−)) model many features of Dravet syndrome, including spontaneous seizures and premature lethality. Scn1a(+/−)mice exhibit variabl...
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| Publicado no: | Exp Neurol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6287761/ https://ncbi.nlm.nih.gov/pubmed/30347190 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2018.10.010 |
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