Oral Feeding of an Antioxidant Cocktail as a Therapeutic Strategy in a Mouse Model of Rett Syndrome: Merits and Limitations of Long-Term Treatment

Rett syndrome (RTT) is a severe neurodevelopmental disorder that typically arises from spontaneous germline mutations in the X-chromosomal methyl-CpG binding protein 2 (MECP2) gene. For the first 6–18 months of life, the development of the mostly female patients appears normal. Subsequently, cogniti...

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Detalles Bibliográficos
Autores principales: Baroncelli, Laura, Auel, Stefanie, Rinne, Lena, Schuster, Ann-Kathrin, Brand, Victoria, Kempkes, Belinda, Dietrich, Katharina, Müller, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311910/
https://www.ncbi.nlm.nih.gov/pubmed/35883897
http://dx.doi.org/10.3390/antiox11071406

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9311910/
https://www.ncbi.nlm.nih.gov/pubmed/35883897
http://dx.doi.org/10.3390/antiox11071406

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