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Substantial acetylcholine reduction in multiple brain regions of Mecp2-deficient female rats and associated behavioral abnormalities
Rett syndrome (RTT) is a neurodevelopmental disorder with X-linked dominant inheritance caused mainly by mutations in the methyl-CpG-binding protein 2 (MECP2) gene. The effects of various Mecp2 mutations have been extensively assessed in mouse models, but none adequately mimic the symptoms and patho...
Autores principales: | Murasawa, Hiroyasu, Kobayashi, Hiroyuki, Imai, Jun, Nagase, Takahiko, Soumiya, Hitomi, Fukumitsu, Hidefumi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8530288/ https://www.ncbi.nlm.nih.gov/pubmed/34673817 http://dx.doi.org/10.1371/journal.pone.0258830 |
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