Genome-wide screening for genes involved in the epigenetic basis of fragile X syndrome

Fragile X syndrome (FXS), the most prevalent heritable form of intellectual disability, is caused by the transcriptional silencing of the FMR1 gene. The epigenetic factors responsible for FMR1 inactivation are largely unknown. Here, we initially demonstrated the feasibility of FMR1 reactivation by t...

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Detalles Bibliográficos
Autores principales: Vershkov, Dan, Yilmaz, Atilgan, Yanuka, Ofra, Nielsen, Anders Lade, Benvenisty, Nissim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133649/
https://www.ncbi.nlm.nih.gov/pubmed/35427485
http://dx.doi.org/10.1016/j.stemcr.2022.03.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133649/
https://www.ncbi.nlm.nih.gov/pubmed/35427485
http://dx.doi.org/10.1016/j.stemcr.2022.03.011

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