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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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| Publicado no: | Neuroscience |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | 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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