UTRN and Duchenne muscular dystrophy: The aim of this study was to further establish and compare the bone structure and function, BMAT quantity, and growth phenotypes of the mdx, mdx:Utrn+/− and mdx:Cmah−/− DMD mouse models with the C57BL/10 wild-type (WT) mouse, and determine which model would most closely mimic the clinical characteristics of DMD.