Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular Dysfunctions

Rett syndrome (RTT) and Fragile X syndrome (FXS) are two monogenetic neurodevelopmental disorders with complex clinical presentations. RTT is caused by mutations in the Methyl-CpG binding protein 2 gene (MECP2) altering the function of its protein product MeCP2. MeCP2 modulates gene expression by bi...

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Detalles Bibliográficos
Autores principales: Bach, Snow, Shovlin, Stephen, Moriarty, Michael, Bardoni, Barbara, Tropea, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640214/
https://www.ncbi.nlm.nih.gov/pubmed/34867203
http://dx.doi.org/10.3389/fncel.2021.764761

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8640214/
https://www.ncbi.nlm.nih.gov/pubmed/34867203
http://dx.doi.org/10.3389/fncel.2021.764761

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