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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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| Hauptverfasser: | , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Society for Neuroscience
2013
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| Schlagworte: | |
| Online Zugang: | 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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