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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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| Publicado en: | Mol Genet Metab |
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| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2016
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| Assuntos: | |
| Acceso en liña: | 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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