MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases. Townend, G., S., Ehrhart, F., van Kranen, H., J., Wilkinson, M., Jacobsen, A., Roos, M., Willighagen, E., L., van Enckevort, D., Evelo, C., T., & Curfs, L., M., G. Human Mutation, 39(7):914-924, 7, 2018.
MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases [link]Website  bibtex   
@article{
 title = {MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases},
 type = {article},
 year = {2018},
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 pages = {914-924},
 volume = {39},
 websites = {http://doi.wiley.com/10.1002/humu.23542},
 month = {7},
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 created = {2018-09-02T13:34:04.300Z},
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 last_modified = {2018-10-15T08:36:22.870Z},
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 citation_key = {Townend2018},
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 bibtype = {article},
 author = {Townend, Gillian S. and Ehrhart, Friederike and van Kranen, Henk J. and Wilkinson, Mark and Jacobsen, Annika and Roos, Marco and Willighagen, Egon L. and van Enckevort, David and Evelo, Chris T. and Curfs, Leopold M. G.},
 journal = {Human Mutation},
 number = {7}
}

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