Caricamento...
Accelerated Hyper-Maturation of Parvalbumin Circuits in the Absence of MeCP2
Methyl-CpG-binding protein 2 (MeCP2) mutations are the primary cause of Rett syndrome, a severe neurodevelopmental disorder. Cortical parvalbumin GABAergic interneurons (PV) make exuberant somatic connections onto pyramidal cells in the visual cortex of Mecp2-deficient mice, which contributes to sil...
Salvato in:
| Pubblicato in: | Cereb Cortex |
|---|---|
| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2020
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7029683/ https://ncbi.nlm.nih.gov/pubmed/31038696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhz085 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|