FMRP Interacts with RARα in Synaptic Retinoic Acid Signaling and Homeostatic Synaptic Plasticity

The fragile X syndrome (FXS) is an X-chromosome-linked neurodevelopmental disorder with severe intellectual disability caused by inactivation of the fragile X mental retardation 1 (<i>FMR1</i>) gene and subsequent loss of the fragile X mental retardation protein (FMRP). Among the various...

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Bibliographic Details
Main Authors: Esther Park, Anthony G. Lau, Kristin L. Arendt, Lu Chen
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/12/6579