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Astrocytes and Lysosomal Storage Diseases
Lysosomal storage diseases (LSDs) encompass a wide range of disorders characterized by inborn errors of lysosomal function. The majority of LSDs result from genetic defects in lysosomal enzymes, although some arise from mutations in lysosomal proteins that lack known enzymatic activity. Neuropatholo...
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| Veröffentlicht in: | Neuroscience |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4664580/ https://ncbi.nlm.nih.gov/pubmed/26037807 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2015.05.061 |
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