RNA sequencing using mouse telencephalon

To identify the RNA expression profile of mouse telencephalon at E14.5 in the presence and absence of FMRP, an RNA binding protein which its absence is the main cause of the neurodevelopmental disorder, fragile X syndrome. RNA sequencing was performed using the RNA extracted from male WT and Fmr1-KO, female WT, Fmr1-het, and Fmr1-KO mouse telencephalon at E14.5.