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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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Bach, Gideon, Eisenberg, Frank, Cantz, Michael, Neufeld, Elizabeth F.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1973
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC433682/
https://ncbi.nlm.nih.gov/pubmed/4269173
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