Oligodendrocyte Lineage Cells Contribute Unique Features to Rett Syndrome Neuropathology

Mutations in the methyl-CpG binding protein 2 gene, Mecp2, affect primarily the brain and lead to a wide range of neuropsychiatric disorders, most commonly Rett syndrome (RTT). Although the neuropathology of RTT is well understood, the cellular and molecular mechanism(s), which lead to the disease i...

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Detalhes bibliográficos
Main Authors: Nguyen, Minh Vu Chuong, Felice, Christy A., Du, Fang, Covey, Matthew V., Robinson, John K., Mandel, Gail, Ballas, Nurit
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3841446/
https://ncbi.nlm.nih.gov/pubmed/24285883
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2657-13.2013
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