Additional file 2: of RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome

List of significant genes (p < 0.05) identified as RTT hits along with references. Information on WT and Mecp2 Jae/y FPKM values, Log2 fold change expression, p-value and q-value (FDR) are provided per respective gene (based on NCBI designation). The directions of expression for the RTT hits observed in previous studies (with references) are also provided. File format: Microsoft Excel spreadsheet. (XLS 34 kb)