Establishment of Glycosaminoglycan Assays for Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders caused by deficiency of the lysosomal enzymes essential for catabolism of glycosaminoglycans (GAGs). Accumulation of undegraded GAGs results in dysfunction of multiple organs, resulting in distinct clinical manifestations. A rang...

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Hlavní autoři: Tomatsu, Shunji, Shimada, Tsutomu, Mason, Robert W., Montaño, Adriana M., Kelly, Joan, LaMarr, William A., Kubaski, Francyne, Giugliani, Roberto, Guha, Aratrik, Yasuda, Eriko, Mackenzie, William, Yamaguchi, Seiji, Suzuki, Yasuyuki, Orii, Tadao
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI 2014
Témata:
Review
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4192686/
https://ncbi.nlm.nih.gov/pubmed/25116756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/metabo4030655
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