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Hyperexcitability and Homeostasis in Fragile X Syndrome

Fragile X Syndrome (FXS) is a leading inherited cause of autism and intellectual disability, resulting from a mutation in the FMR1 gene and subsequent loss of its protein product FMRP. Despite this simple genetic origin, FXS is a phenotypically complex disorder with a range of physical and neurocogn...

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Detalles Bibliográficos
Autores principales: Liu, Xiaopeng, Kumar, Vipendra, Tsai, Nien-Pei, Auerbach, Benjamin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8770333/
https://www.ncbi.nlm.nih.gov/pubmed/35069112
http://dx.doi.org/10.3389/fnmol.2021.805929