Transcriptomic and Epigenomic Landscape in Rett Syndrome

Rett syndrome (RTT) is an extremely invalidating, cureless, developmental disorder, and it is considered one of the leading causes of intellectual disability in female individuals. The vast majority of RTT cases are caused by de novo mutations in the X-linked Methyl-CpG binding protein 2 (MECP2) gen...

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Detalles Bibliográficos
Autores principales: Marano, Domenico, Fioriniello, Salvatore, D’Esposito, Maurizio, Della Ragione, Floriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301932/
https://www.ncbi.nlm.nih.gov/pubmed/34209228
http://dx.doi.org/10.3390/biom11070967

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301932/
https://www.ncbi.nlm.nih.gov/pubmed/34209228
http://dx.doi.org/10.3390/biom11070967

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