The exon-52-deleted mdx52 mouse is a critical model of Duchenne muscular dystrophy (DMD). as it features a deletion in a hotspot region of the DMD gene. frequently mutated in patients. Deletion of exon 52 impedes expression of several brain dystrophins (Dp427. https://www.roneverhart.com/HP-ENVY-TE01-4147c-Desktop-Intel-Core-i7-13700-2-1-GHz-Intel-UHD-Graphics-770-32GB-DDR4-512GB-SSD-1TB-HDD-Windows-11-/