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Therapeutic approaches for lysosomal storage diseases
The lysosomal storage disorders (LSDs) comprise a heterogeneous group of inborn errors of metabolism characterized by tissue substrate deposits, most often caused by a deficiency of the enzyme normally responsible for catabolism of various byproducts of cellular turnover. Individual entities are typ...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3474616/ https://ncbi.nlm.nih.gov/pubmed/23148162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2042018810384429 |
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