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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2011
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| 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 |