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Lysosomal Lipid Storage Diseases
Lysosomal lipid storage diseases, or lipidoses, are inherited metabolic disorders in which typically lipids accumulate in cells and tissues. Complex lipids, such as glycosphingolipids, are constitutively degraded within the endolysosomal system by soluble hydrolytic enzymes with the help of lipid bi...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2011
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3098676/ https://ncbi.nlm.nih.gov/pubmed/21502308 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a004804 |
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