Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

A group of post-natal neurodevelopmental disorders collectively referred to as MeCP2 disorders are caused by aberrations in the gene encoding methyl-CpG-binding protein 2 (MECP2). Loss of MeCP2 function causes Rett syndrome (RTT), whereas increased copy number of the gene causes MECP2 duplication or...

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Detalles Bibliográficos
Autores principales: Ben-Shachar, Shay, Chahrour, Maria, Thaller, Christina, Shaw, Chad A., Zoghbi, Huda Y.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694691/
https://www.ncbi.nlm.nih.gov/pubmed/19369296
http://dx.doi.org/10.1093/hmg/ddp181

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694691/
https://www.ncbi.nlm.nih.gov/pubmed/19369296
http://dx.doi.org/10.1093/hmg/ddp181

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