Meta-Analysis Identifies BDNF and Novel Common Genes Differently Altered in Cross-Species Models of Rett Syndrome

Rett syndrome (RTT) is a rare disorder and one of the most abundant causes of intellectual disabilities in females. Single mutations in the gene coding for methyl-CpG-binding protein 2 (MeCP2) are responsible for the disorder. MeCP2 regulates gene expression as a transcriptional regulator as well as...

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Detalles Bibliográficos
Autores principales: Haase, Florencia, Singh, Rachna, Gloss, Brian, Tam, Patrick, Gold, Wendy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570315/
https://www.ncbi.nlm.nih.gov/pubmed/36232428
http://dx.doi.org/10.3390/ijms231911125

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570315/
https://www.ncbi.nlm.nih.gov/pubmed/36232428
http://dx.doi.org/10.3390/ijms231911125

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