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Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes
View ORCID ProfileFriederike Ehrhart, View ORCID ProfileSusan L.M. Coort, Elisa Cirillo, Eric Smeets, View ORCID ProfileChris T. Evelo, Leopold M. Curfs
doi: https://doi.org/10.1101/062786
Friederike Ehrhart
1Governor Kremers Centre – Rett Expertise Centre, Maastricht University Medical Center, Maastricht, The Netherlands
2Department of Bioinformatics, NUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands
Susan L.M. Coort
2Department of Bioinformatics, NUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands
Elisa Cirillo
2Department of Bioinformatics, NUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands
Eric Smeets
1Governor Kremers Centre – Rett Expertise Centre, Maastricht University Medical Center, Maastricht, The Netherlands
Chris T. Evelo
1Governor Kremers Centre – Rett Expertise Centre, Maastricht University Medical Center, Maastricht, The Netherlands
2Department of Bioinformatics, NUTRIM School for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands
Leopold M. Curfs
1Governor Kremers Centre – Rett Expertise Centre, Maastricht University Medical Center, Maastricht, The Netherlands
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Posted July 08, 2016.
Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes
Friederike Ehrhart, Susan L.M. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, Leopold M. Curfs
bioRxiv 062786; doi: https://doi.org/10.1101/062786
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