Developmental changes in brain activity of heterozygous Scn1a knockout rats

INTRODUCTION: Dravet syndrome (DS) is an infantile-onset developmental and epileptic encephalopathy characterized by an age-dependent evolution of drug-resistant seizures and poor developmental outcomes. Functional impairment of gamma-aminobutyric acid (GABA)ergic interneurons due to loss-of-functio...

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Detalles Bibliográficos
Autores principales: Tahara, Mayu, Higurashi, Norimichi, Hata, Junichi, Nishikawa, Masako, Ito, Ken, Hirose, Shinichi, Kaneko, Takehito, Mashimo, Tomoji, Sakuma, Tetsushi, Yamamoto, Takashi, Okano, Hirotaka James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043303/
https://www.ncbi.nlm.nih.gov/pubmed/36998780
http://dx.doi.org/10.3389/fneur.2023.1125089

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043303/
https://www.ncbi.nlm.nih.gov/pubmed/36998780
http://dx.doi.org/10.3389/fneur.2023.1125089

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