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Dive into the research topics of 'Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor'. Together they form a unique fingerprint.- Sort by
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M.J. Lyst, R. Ekiert, D.H. Ebert, C. Merusi, J. Nowak, J. Selfridge, J. Guy, N.R. Kastan, N.D. Robinson, F. de Lima Alves, J. Rappsilber, M.E. Greenberg, A. Bird
Research output: Contribution to journal › Article › peer-review