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Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome
Rett syndrome (RTT) is one of the most prevalent female neurodevelopmental disorders that cause severe mental retardation. Mutations in methyl CpG binding protein 2 (MeCP2) are mainly responsible for RTT. Patients with classical RTT exhibit normal development until age 6–18 mo, at which point they b...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3161557/ https://ncbi.nlm.nih.gov/pubmed/21807996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1018979108 |
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