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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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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2020
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| Assuntos: | |
| Acesso em linha: | 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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