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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
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 |
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