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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Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: MDPI 2014
Matèries:
Review
Accés en línia: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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