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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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Detalhes bibliográficos
Main Authors: Schulze, Heike, Sandhoff, Konrad
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2011
Assuntos:
Acesso em linha: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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