Chronic rare DUX4 expression in mouse drives transcriptional similarities to human FSHD in whole muscle and fibroadiopgenic progenitors. Chronic rare DUX4 expression in mouse drives transcriptional similarities to human FSHD in whole muscle and fibroadiopgenic progenitors

RNA-seq data was obtained on various samples from the iDUX4pA mouse model for FSHD and from control WT littermates. Overall design: RNA-seq was performed on whole muscle, as well as sorted endothelial cells and fibroadipogenic progenitors at early and late time points in the course of the disease.