Article
Astrocytic contribution to auditory hypersensitivity in a mouse model of fragile X syndrome
2025-02-18
Abstract excerpt
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and a leading cause of autism spectrum disorder (ASD). FXS is caused by mutations in the fragile X messenger ribonucleoprotein gene 1 ( FMR1 ), which result in complete or partial loss of expression of its protein product, fragile X messenger ribonucleoprotein (FMRP). Neuronal impairments in the absence of FMRP have been extensi...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- 40175c95-f74b-5978-b020-eb344e6733e6
- DOI
- 10.1101/2025.02.14.638346
