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

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

DOI Full Paper Access

397

Citations

35

References

2013

Year

Matthew J. Lyst, Robert Ekiert, Daniel H. Ebert, Cara Merusi, Jakub Nowak, Jim Selfridge, Jacky Guy, Nathaniel R. Kastan, Nathaniel D. Robinson, Flávia de Lima Alves,

Nature Neuroscience

Signal TransductionMendelian DisorderRett Syndrome MutationsGenetic DisorderGeneticsMolecular BiologyNcor/smrt Co-repressorMolecular GeneticsMedicineCell Signaling

References

	Year	Citations

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