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Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome
Dravet Syndrome (DS) is a severe neurodevelopmental disorder caused by pathogenic loss of function variants in the gene SCN1A which encodes the voltage gated sodium (Na(+)) channel subunit Nav1.1. GABAergic interneurons expressing parvalbumin (PV-INs) and somatostatin (SST-INs) exhibit impaired exci...
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| Publicado no: | eLife |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
eLife Sciences Publications, Ltd
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6629374/ https://ncbi.nlm.nih.gov/pubmed/31282864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.46846 |
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