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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

ChromatinGenome InstabilityTranscriptional RegulationMendelian DisorderX-linked Mecp2Disease MechanismMethyl-cpg-binding Protein 2Rett SyndromeGeneticsGenetic DisorderMolecular BiologyMolecular GeneticsMedicineEpigenetics