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The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate Sulfatase
Skin fibroblasts cultured from patients affected with the Hunter syndrome are deficient in the activity of a protein, named the “Hunter corrective factor,” that is required for degradation of dermatan and heparan sulfates. We now show that this factor, purified from human urine, removes about 2% of...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
1973
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC433682/ https://ncbi.nlm.nih.gov/pubmed/4269173 |
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