Associated Papers
The Molecular Basis of MeCP2 Function in the Brain.
Tillotson R et al.
Journal of Molecular Biology, 2020
From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.
Sheikh TI et al.
Scientific Reports, 2016
Binding Analysis of Methyl-CpG Binding Domain of MeCP2 and Rett Syndrome Mutations.
Yang Y et al.
Acs Chemical Biology, 2016
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