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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...

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Literature Corpus work
40175c95-f74b-5978-b020-eb344e6733e6
DOI
10.1101/2025.02.14.638346
Open publication

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Astrocytic contribution to auditory hypersensitivity in a mouse model of fragile X syndromeDOI 10.1101/2025.02.14.638346
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