Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain

BACKGROUND: Rett syndrome (RTT, MIM #312750) is a severe neurological disorder caused by mutations in the X-linked methyl-CpG binding protein 2 (MECP2) gene. Female patients are affected with an incidence of 1/15000 live births and develop normally from birth to 6-18 months of age before the onset o...

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Detalles Bibliográficos
Autores principales: Panayotis, Nicolas, Ghata, Adeline, Villard, Laurent, Roux, Jean-Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112112/
https://www.ncbi.nlm.nih.gov/pubmed/21609470
http://dx.doi.org/10.1186/1471-2202-12-47

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112112/
https://www.ncbi.nlm.nih.gov/pubmed/21609470
http://dx.doi.org/10.1186/1471-2202-12-47

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