Nalaganje...
MeCP2 Deficiency Leads to Loss of Glial Kir4.1
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder usually caused by mutations in methyl-CpG-binding protein 2 (MeCP2). RTT is typified by apparently normal development until 6–18 mo of age, when motor and communicative skills regress and hand stereotypies, autonomic symptoms, and seizur...
Shranjeno v:
| izdano v: | eNeuro |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Society for Neuroscience
2018
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5818552/ https://ncbi.nlm.nih.gov/pubmed/29464197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0194-17.2018 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|