Browsing Scholarly Works, Fralin Biomedical Research Institute at VTC by Subject "Sequence Analysis, RNA"
Now showing items 1-1 of 1
RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome. (2017)BACKGROUND: Rett syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the transcriptional regulator MeCP2. Much of our understanding of MeCP2 function is derived from transcriptomic studies with ...