Article
Activity-Induced MeCP2 Phosphorylation Regulates Retinogeniculate Synapse Refinement
2023-07-03
Abstract excerpt
<h4>ABSTRACT</h4> Mutations in MECP2 give rise to Rett syndrome (RTT), an X-linked neurodevelopmental disorder that results in broad cognitive impairments in females. While the exact etiology of RTT symptoms remains unknown, one possible explanation for its clinical presentation is that loss of MeCP2 causes miswiring of neural circuits due to defects in the brain’s capacity to respond to changes in neuronal acti...
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Identifiers and source
- Literature Corpus work
- 9c51fc3a-a2f2-51cb-83bf-ba43d244e7f7
- DOI
- 10.1101/2023.07.03.547549
