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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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S. Kudo

Hokkaido Institute of Public Health

060-0819

Sapporo

Japan

[email]@*.*.hokkaido.jp

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Affiliation

Hokkaido Institute of Public Health, 060-0819, Sapporo, Japan. 2001 - 2003

References

Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain. Kudo, S., Nomura, Y., Segawa, M., Fujita, N., Nakao, M., Schanen, C., Tamura, M. J. Med. Genet. (2003) [Pubmed]
Functional characterisation of MeCP2 mutations found in male patients with X linked mental retardation. Kudo, S., Nomura, Y., Segawa, M., Fujita, N., Nakao, M., Hammer, S., Schanen, C., Terai, I., Tamura, M. J. Med. Genet. (2002) [Pubmed]
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems. Kudo, S., Nomura, Y., Segawa, M., Fujita, N., Nakao, M., Dragich, J., Schanen, C., Tamura, M. Brain Dev. (2001) [Pubmed]