Comprehensive Volumetric Analysis of Mecp2-Null Mouse Model for Rett Syndrome by T2-Weighted 3D Magnetic Resonance Imaging

Rett syndrome (RTT) is a severe progressive neurodevelopmental disorder characterized by various neurological symptoms. Almost all RTT cases are caused by mutations in the X-linked methyl-CpG-binding protein 2 (MeCP2) gene, and several mouse models have been established to understand the disease. Ho...

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Detalles Bibliográficos
Autores principales: Akaba, Yuichi, Shiohama, Tadashi, Komaki, Yuji, Seki, Fumiko, Ortug, Alpen, Sawada, Daisuke, Uchida, Wataru, Kamagata, Koji, Shimoji, Keigo, Aoki, Shigeki, Takahashi, Satoru, Suzuki, Takeshi, Natsume, Jun, Takahashi, Emi, Tsujimura, Keita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127869/
https://www.ncbi.nlm.nih.gov/pubmed/35620663
http://dx.doi.org/10.3389/fnins.2022.885335

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127869/
https://www.ncbi.nlm.nih.gov/pubmed/35620663
http://dx.doi.org/10.3389/fnins.2022.885335

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