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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI 2014
Gaiak:
Review
Sarrera elektronikoa: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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