Proteomic and transcriptional changes associated with MeCP2 dysfunction reveal nodes for therapeutic intervention in Rett syndrome
Author:
Funder
National Institutes of Health
NINDS
International Rett Syndrome Foundation
Publisher
Elsevier BV
Subject
Cell Biology,Cellular and Molecular Neuroscience
Reference190 articles.
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4. MeCP2: the long trip from a chromatin protein to neurological disorders;Ausio;Trends Mol. Med.,2014
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