Review highlights non-coding elements regulating muscular dystrophies, suggesting significant genetic roles.
Muscular dystrophies are a class of diseases characterized by muscular weakness, breakdown, and heavily impaired function and quality of life [1]. Numerous types of muscular dystrophy have been identified, with different causative genes and dystrophic mechanisms. While the majority of studies emphasize the protein product encoded by each gene, a growing body of research has identified non-coding elements as key regulators of muscular dystrophy [2,3]. In this review, we summarize the common noncoding mechanisms known to regulate multiple forms of muscular dystrophy. We also highlight individual studies exploring local, disease-specific noncoding elements to each disease. Together, this provides a comprehensive overview of the major role of non-coding regulation in muscular dystrophies.
No takes yet. Share an insight, caveat, or question.
Wilton-Clark et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: