Unconventional Transcriptional Response to Environmental Enrichment in a Mouse Model of Rett Syndrome

BACKGROUND: Rett syndrome (RTT) is an X-linked postnatal neurodevelopmental disorder caused by mutations in the gene encoding methyl-CpG binding protein 2 (MeCP2) and one of the leading causes of mental retardation in females. RTT is characterized by psychomotor retardation, purposeless hand movemen...

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Detalles Bibliográficos
Autores principales: Kerr, Bredford, Silva, Pamela A., Walz, Katherina, Young, Juan I.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902516/
https://www.ncbi.nlm.nih.gov/pubmed/20634955
http://dx.doi.org/10.1371/journal.pone.0011534

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902516/
https://www.ncbi.nlm.nih.gov/pubmed/20634955
http://dx.doi.org/10.1371/journal.pone.0011534

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