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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Detalhes bibliográficos
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: MDPI 2014
Assuntos:
Review
Acesso em linha: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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