SnapShot: Lysosomal Storage Diseases
Copyright policy )SnapShot: Lysosomal Storage Diseases
Lysosomal storage diseases (LSDs) represent a group of monogenic inherited metabolic disorders characterized by the progressive accumulation of undegraded substrates inside lysosomes, resulting in aberrant lysosomal activity and homeostasis. This SnapShot summarizes the intracellular localization and function of proteins implicated in LSDs. Common aspects of LSD pathogenesis and the major current therapeutic approaches are noted. To view this SnapShot, open or download the PDF.
- National Heart Lung and Blood Institute United States
- National Institutes of Health United States
- National Institute of Health Pakistan
- National Institute of Health (NIH/NICHD) United States
Lysosomal Storage Diseases, Eukaryotic Cells, Autophagy, Animals, Homeostasis, Humans, Lysosomes, Lysosomal Membrane Proteins, Enzymes
Lysosomal Storage Diseases, Eukaryotic Cells, Autophagy, Animals, Homeostasis, Humans, Lysosomes, Lysosomal Membrane Proteins, Enzymes
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