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Systemic metabolic remodeling in mucopolysaccharidosis revealed by untargeted urinary metabolomics
Mucopolysaccharidoses (MPS) are lysosomal storage disorders characterized by glycosaminoglycan (GAG) accumulation and progressive multi-organ dysfunction. However, the systemic metabolic consequences of lysosomal dysfunction remain incompletely defined. Untargeted urinary metabolomics was performed using...