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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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192686/
https://www.ncbi.nlm.nih.gov/pubmed/25116756
http://dx.doi.org/10.3390/metabo4030655

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192686/
https://www.ncbi.nlm.nih.gov/pubmed/25116756
http://dx.doi.org/10.3390/metabo4030655

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