Establishment of Glycosaminoglycan Assays for Mucopolysaccharidoses

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...

Full description

Bibliographic Details
Main Authors: Shunji Tomatsu, Tsutomu Shimada, Robert W. Mason, Adriana M. Montaño, Joan Kelly, William A. LaMarr, Francyne Kubaski, Roberto Giugliani, Aratrik Guha, Eriko Yasuda, William Mackenzie, Seiji Yamaguchi, Yasuyuki Suzuki, Tadao Orii
Format: Article
Language:English
Published: MDPI AG 2014-08-01
Series:Metabolites
Subjects:
mucopolysaccharidoses
ELISA
tandem mass spectrometry
glycosaminoglycan
chondroitin sulfate
dermatan sulfate
heparan sulfate
keratan sulfate
Online Access:http://www.mdpi.com/2218-1989/4/3/655

Internet

http://www.mdpi.com/2218-1989/4/3/655

Similar Items