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WGCNA Identifies Translational and Proteasome-Ubiquitin Dysfunction in Rett Syndrome
Rett Syndrome (RTT) is an X linked neurodevelopmental disorder caused by mutations in the methyl-CpG-binding protein 2 (MECP2) gene, resulting in severe cognitive and physical disabilities. Despite an apparent normal prenatal and postnatal development period, symptoms usually present around 6 to 18...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465861/ https://www.ncbi.nlm.nih.gov/pubmed/34576118 http://dx.doi.org/10.3390/ijms22189954 |