A carregar...
Detection of neurophysiological features in female R255X MeCP2 mutation mice
Rett syndrome (RTT) is a severe neurodevelopmental disorder (NDD) that is nearly always caused by loss of function mutations in Methyl-CpG-binding Protein 2 (MECP2) and shares many clinical features with other NDD. Genetic restoration of Mecp2 in symptomatic mice lacking MeCP2 expression can reverse...
Na minha lista:
| Publicado no: | Neurobiol Dis |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7572861/ https://ncbi.nlm.nih.gov/pubmed/32927061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2020.105083 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|