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Similar content being viewed by others Duchenne muscular dystrophy (DMD): an overview Duchenne muscular dystrophy (DMD) represents one of the most common, severe, and lethal types of dystrophinopathies, which are caused by mutations in the X-linked DMD gene that encodes dystrophin, a structural muscle protein

They regulate gene expression through transcription, translation, protein modification, and RNAprotein complexing (107)

249,445,446,447,448,449 Uric acid exerts multifaceted effects on endothelial function and vascular health through its interactions with NO, ROS, and inflammatory pathways, highlighting its potential role in the pathogenesis of cardiovascular diseases like atherosclerosis