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Article

Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation.

Journal of medical genetics - 1 Feb 2002

Kudo S, Nomura Y, Segawa M, Fujita N, Nakao M, Hammer S, Schanen C, Terai I, Tamura M

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Share to Chromosomal Proteins, Non-Histone
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methyl-CpG-Binding Protein 2

Share to Mutagenesis, Site-Directed

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Identifiers

PMID: 11836365
DOI: 10.1136/jmg.39.2.132
PMCID: PMC1735040

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