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/La-Tierra-de-Acre-Mezcal-Espadin-86-proof/