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Dissecting the phenotypes of Dravet syndrome by gene deletion
Neurological and psychiatric syndromes often have multiple disease traits, yet it is unknown how such multi-faceted deficits arise from single mutations. Haploinsufficiency of the voltage-gated sodium channel Na(v)1.1 causes Dravet syndrome, an intractable childhood-onset epilepsy with hyperactivity...
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| Veröffentlicht in: | Brain |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5022661/ https://ncbi.nlm.nih.gov/pubmed/26017580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awv142 |
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