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Mucopolysaccharidosis IVA and glycosaminoglycans
Mucopolysaccharidosis IVA (MPS IVA; Morquio A: OMIM 253000) is a lysosomal storage disease with an autosomal recessive trait caused by the deficiency of N-acetylgalactosamine-6-sulfate sulfatase. Deficiency of this enzyme leads to accumulation of specific glycosaminoglycans (GAGs): chondroitin-6-sul...
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| Publicado no: | Mol Genet Metab |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5293636/ https://ncbi.nlm.nih.gov/pubmed/27979613 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2016.11.007 |
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