Interregulation between fragile X mental retardation protein and methyl CpG binding protein 2 in the mouse posterior cerebral cortex

Several X-linked neurodevelopmental disorders including Rett syndrome, induced by mutations in the MECP2 gene, and fragile X syndrome (FXS), caused by mutations in the FMR1 gene, share autism-related features. The mRNA coding for methyl CpG binding protein 2 (MeCP2) has previously been identified as...

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Detalles Bibliográficos
Autores principales: Arsenault, Jason, Hooper, Alexander W M, Gholizadeh, Shervin, Kong, Tian, Pacey, Laura K, Koxhioni, Enea, Niibori, Yosuke, Eubanks, James H, Wang, Lu-Yang, Hampson, David R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
General Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861017/
https://www.ncbi.nlm.nih.gov/pubmed/33084871
http://dx.doi.org/10.1093/hmg/ddaa226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861017/
https://www.ncbi.nlm.nih.gov/pubmed/33084871
http://dx.doi.org/10.1093/hmg/ddaa226

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