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Chondroitin sulfate and growth factor signaling in the skeleton: Possible links to MPS VI
Mucopolysaccharidosis type VI (MPS VI), also called Maroteaux-Lamy syndrome, is an autosomal recessive lysosomal storage disorder caused by deficiency of a specific enzyme required for glycosaminoglycan catabolism. Deficiency in the N-acetylgalactosamine-4-sulfatase (4S) enzyme, also called arylsulf...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2901997/ https://ncbi.nlm.nih.gov/pubmed/20628554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PRM-2010-0117 |
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