Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative Trolox

Rett syndrome (RTT) is a severe neurodevelopmental disorder typically arising from spontaneous mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. The almost exclusively female Rett patients show an apparently normal development during their first 6–18 months of life. Subsequen...

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Detalles Bibliográficos
Autores principales: Janc, Oliwia A., Hüser, Marc A., Dietrich, Katharina, Kempkes, Belinda, Menzfeld, Christiane, Hülsmann, Swen, Müller, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109403/
https://www.ncbi.nlm.nih.gov/pubmed/27895554
http://dx.doi.org/10.3389/fncel.2016.00266

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109403/
https://www.ncbi.nlm.nih.gov/pubmed/27895554
http://dx.doi.org/10.3389/fncel.2016.00266

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