Proteomic Analysis in Morquio A Cells Treated with Immobilized Enzymatic Replacement Therapy on Nanostructured Lipid Systems

Morquio A syndrome, or mucopolysaccharidosis type IVA (MPS IVA), is a lysosomal storage disease due to mutations in the N-acetylgalactosamine-6-sulfatase (GALNS) gene. Systemic skeletal dysplasia and the related clinical features of MPS IVA are due to disruption of cartilage and its extracellular ma...

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Pubblicato in:Int J Mol Sci
Autori principali: Álvarez, J. Víctor, Bravo, Susana B., García-Vence, María, De Castro, María J., Luzardo, Asteria, Colón, Cristóbal, Tomatsu, Shunji, Otero-Espinar, Francisco J., Couce, María L.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2019
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6769449/
https://ncbi.nlm.nih.gov/pubmed/31540344
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184610
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