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Unexpected cellular players in Rett syndrome pathology

Rett syndrome is a devastating neurodevelopmental disorder, primarily caused by mutations of methyl CpG-binding protein 2 (MeCP2). Although the genetic cause of disease was identified over a decade ago, a significant gap still remains in both our clinical and scientific understanding of its pathogen...

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Bibliografische gegevens
Gepubliceerd in:Neurobiol Dis
Hoofdauteurs: Cronk, James C., Derecki, Noel, Litvak, Vladimir, Kipnis, Jonathan
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2015
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4644494/
https://ncbi.nlm.nih.gov/pubmed/25982834
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2015.05.005
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