Molecular Context-Dependent Effects Induced by Rett Syndrome-Associated Mutations in MeCP2

Methyl-CpG binding protein 2 (MeCP2) is a transcriptional regulator and a chromatin-binding protein involved in neuronal development and maturation. Loss-of-function mutations in MeCP2 result in Rett syndrome (RTT), a neurodevelopmental disorder that is the main cause of mental retardation in female...

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Detalles Bibliográficos
Autores principales: Ortega-Alarcon, David, Claveria-Gimeno, Rafael, Vega, Sonia, Jorge-Torres, Olga C., Esteller, Manel, Abian, Olga, Velazquez-Campoy, Adrian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696773/
https://www.ncbi.nlm.nih.gov/pubmed/33182787
http://dx.doi.org/10.3390/biom10111533

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696773/
https://www.ncbi.nlm.nih.gov/pubmed/33182787
http://dx.doi.org/10.3390/biom10111533

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