Impaired Functional Connectivity Underlies Fragile X Syndrome

Fragile X syndrome (FXS), the most common form of inherited intellectual disability, is caused by a developmentally regulated silencing of the FMR1 gene, but its effect on human neuronal network development and function is not fully understood. Here, we isolated isogenic human embryonic stem cell (h...

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Detalles Bibliográficos
Autores principales: Gildin, Lital, Rauti, Rossana, Vardi, Ofir, Kuznitsov-Yanovsky, Liron, Maoz, Ben M., Segal, Menahem, Ben-Yosef, Dalit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878121/
https://www.ncbi.nlm.nih.gov/pubmed/35216162
http://dx.doi.org/10.3390/ijms23042048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878121/
https://www.ncbi.nlm.nih.gov/pubmed/35216162
http://dx.doi.org/10.3390/ijms23042048

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