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    Cerebellar gene expression data from Mecp2-null and MECP2-transgenic mice

    (Submitter supplied) We compared gene expression changes in the cerebellum of mice lacking MeCP2 (Mecp2-null) and mice overexpressing MeCP2 (MECP2-transgenic). A group of postnatal neurodevelopmental disorders collectively referred to as MeCP2 disorders are caused by aberrations in the gene encoding methyl-CpG-binding protein 2 (MECP2). Loss of MeCP2 function causes Rett syndrome (RTT), whereas increased copy number of the gene causes MECP2 duplication or triplication syndromes. more...
    Organism:
    Mus musculus
    Type:
    Expression profiling by array
    Platform:
    GPL6193
    20 Samples
    Download data:
    GEO (CEL)
    Series
    Accession:
    GSE15574
    ID:
    200015574

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