Fragile X Syndrome as an interneuronopathy: a lesson for future studies and treatments

Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability (ID) and a primary genetic cause of autism spectrum disorder (ASD). FXS arises from the silencing of the FMR1 gene causing the lack of translation of its encoded protein, the Fragile X Messenger RibonucleoProtein (...

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Detalles Bibliográficos
Autores principales: Tempio, Alessandra, Boulksibat, Asma, Bardoni, Barbara, Delhaye, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176609/
https://www.ncbi.nlm.nih.gov/pubmed/37188005
http://dx.doi.org/10.3389/fnins.2023.1171895

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176609/
https://www.ncbi.nlm.nih.gov/pubmed/37188005
http://dx.doi.org/10.3389/fnins.2023.1171895

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