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...

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Detalles Bibliográficos
Autores principales: Urdinguio, Rocio G., Lopez-Serra, Lidia, Lopez-Nieva, Pilar, Alaminos, Miguel, Diaz-Uriarte, Ramon, Fernandez, Agustin F., Esteller, Manel
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Research Article
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

Internet

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

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