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Accelerated Hyper-Maturation of Parvalbumin Circuits in the Absence of MeCP2
Methyl-CpG-binding protein 2 (MeCP2) mutations are the primary cause of Rett syndrome, a severe neurodevelopmental disorder. Cortical parvalbumin GABAergic interneurons (PV) make exuberant somatic connections onto pyramidal cells in the visual cortex of Mecp2-deficient mice, which contributes to sil...
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| 出版年: | Cereb Cortex |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7029683/ https://ncbi.nlm.nih.gov/pubmed/31038696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhz085 |
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