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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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Literature Corpus work
9c51fc3a-a2f2-51cb-83bf-ba43d244e7f7
DOI
10.1101/2023.07.03.547549
Open publication

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Activity-Induced MeCP2 Phosphorylation Regulates Retinogeniculate Synapse RefinementDOI 10.1101/2023.07.03.547549
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