Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses

Mucopolysaccharidoses (MPSs) and mucolipidoses (ML) are groups of lysosomal storage disorders in which lysosomal hydrolases are deficient leading to accumulation of undegraded glycosaminoglycans (GAGs), throughout the body, subsequently resulting in progressive damage to multiple tissues and organs....

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Vydáno v:Mol Genet Metab
Hlavní autoři: Kubaski, Francyne, Suzuki, Yasuyuki, Orii, Kenji, Giugliani, Roberto, Church, Heather J., Mason, Robert W., Dũng, Vũ Chí, Ngoc, Can Thi Bich, Yamaguchi, Seiji, Kobayashi, Hironori, Girisha, Katta M., Fukao, Toshiyuki, Orii, Tadao, Tomatsu, Shunji
Médium: Artigo
Jazyk:Inglês
Vydáno: 2016
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5346460/
https://ncbi.nlm.nih.gov/pubmed/28065440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.12.010
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