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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...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3112112/ https://ncbi.nlm.nih.gov/pubmed/21609470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2202-12-47 |
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