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Neuronal Morphology in MeCP2 Mouse Models is Intrinsically Variable and Depends on Age, Cell type, and Mecp2 Mutation
Rett Syndrome (RTT), a progressive neurological disorder characterized by developmental regression and loss of motor and language skills, is caused by mutations in the X-linked gene encoding methyl-CpG binding protein 2 (MECP2). Neurostructural phenotypes including decreased neuronal size, dendritic...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3748238/ https://ncbi.nlm.nih.gov/pubmed/23659895 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2013.04.020 |
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