Cargando…
Altered synaptic connectivity in an in vitro human model of STXBP1 encephalopathy
Early infantile developmental and epileptic encephalopathies are devastating conditions, generally of genetic origin, but the pathological mechanisms often remain obscure. A major obstacle in this field of research is the difficulty of studying cortical brain development in humans, at the relevant t...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2022
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9976961/ https://www.ncbi.nlm.nih.gov/pubmed/36315647 http://dx.doi.org/10.1093/brain/awac396 |