Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

Mucopolysaccharidosis type IVA (MPS IVA) is a lysosomal storage disease caused by mutations in the N-acetylgalactosamine-6-sulfatase (GALNS) gene. Skeletal dysplasia and the related clinical features of MPS IVA are caused by disruption of the cartilage and its extracellular matrix, leading to a grow...

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Detaylı Bibliyografya
Yayımlandı:Int J Mol Sci
Asıl Yazarlar: Álvarez, Víctor J., Bravo, Susana B., Chantada-Vazquez, Maria Pilar, Colón, Cristóbal, De Castro, María J., Morales, Montserrat, Vitoria, Isidro, Tomatsu, Shunji, Otero-Espinar, Francisco J., Couce, María L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2020
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7795692/
https://ncbi.nlm.nih.gov/pubmed/33379360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22010226
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