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Mecp2-Null Mice Provide New Neuronal Targets for Rett Syndrome
BACKGROUND: Rett syndrome (RTT) is a complex neurological disorder that is one of the most frequent causes of mental retardation in women. A great landmark in research in this field was the discovery of a relationship between the disease and the presence of mutations in the gene that codes for the m...
| Autores principales: | , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2008
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2576441/ https://www.ncbi.nlm.nih.gov/pubmed/18989361 http://dx.doi.org/10.1371/journal.pone.0003669 |