Loading...
The MeCP2E1/E2-BDNF-miR132 Homeostasis Regulatory Network Is Region-Dependent in the Human Brain and Is Impaired in Rett Syndrome Patients
Rett Syndrome (RTT) is a rare and progressive neurodevelopmental disorder that is caused by de novo mutations in the X-linked Methyl CpG binding protein 2 (MECP2) gene and is subjected to X-chromosome inactivation. RTT is commonly associated with neurological regression, autistic features, motor con...
Saved in:
| Published in: | Front Cell Dev Biol |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Frontiers Media S.A.
2020
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7471663/ https://ncbi.nlm.nih.gov/pubmed/32974336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.00763 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|