Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.
Lyst MJ; Ekiert R; Ebert DH; Merusi C; Nowak J; Selfridge J; Guy J; Kastan NR; Robinson ND; de Lima Alves F; Rappsilber J; Greenberg ME; Bird A; Nature Neuroscience, 2013, vol. 16, issue 7, p 898, ISSN 15461726. ISBN 15461726.

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