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Functional consequences of Rett syndrome mutations on human MeCP2.
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Functional consequences of Rett syndrome mutations on human MeCP2.
Yusufzai TM, Wolffe AP. Functional consequences of Rett syndrome mutations on human MeCP2. Nucleic Acids Res. 2000 Nov 01; 28(21):4172-9.
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PubMed
subject areas
Amino Acid Sequence
Amino Acid Substitution
Animals
Cell Line
Chromosomal Proteins, Non-Histone
DNA Methylation
DNA-Binding Proteins
Down-Regulation
Genotype
Humans
Methyl-CpG-Binding Protein 2
Molecular Sequence Data
Mutation, Missense
Oocytes
Phenotype
Protein Binding
Protein Structure, Tertiary
Recombinant Proteins
Repressor Proteins
Rett Syndrome
Sequence Alignment
Substrate Specificity
Transfection
Xenopus laevis