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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Schulze, Heike, Sandhoff, Konrad
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Cold Spring Harbor Laboratory Press 2011
Gaiak:
Sarrera elektronikoa: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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