Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor

author
created [InstanceEdit:9005571] Orlic-Milacic, Marija, 2017-05-09
dbId 9005556
displayName Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
journal Nat. Neurosci.
pages 898-902
pubMedIdentifier 23770565
schemaClass LiteratureReference
title Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor
url http://www.ncbi.nlm.nih.gov/pubmed/23770565
volume 16
year 2013
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