Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease

Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients displaying neurological regression and autism spectrum features. The affected individuals are primarily young females, and more than 95% of patients carry de novo mutation(s) in the Methyl-CpG-Binding Protein...

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Detalles Bibliográficos
Autores principales: Pejhan, Shervin, Rastegar, Mojgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827577/
https://www.ncbi.nlm.nih.gov/pubmed/33429932
http://dx.doi.org/10.3390/biom11010075

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827577/
https://www.ncbi.nlm.nih.gov/pubmed/33429932
http://dx.doi.org/10.3390/biom11010075

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