B4GALNT2 and Duchenne muscular dystrophy: An alternative strategy to target a DMD/muscle damage-related pathway was also proposed by Kevin Flanigan in a recent ongoing clinical trial, utilizing AAV delivery of beta-1,4 N-acetylgalactosaminyltransferase 2 (GALGT2), a GalNac glycosyltransferase (NCT03333590).