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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Udgivet i:Proc Natl Acad Sci U S A
Main Authors: Bach, Gideon, Eisenberg, Frank, Cantz, Michael, Neufeld, Elizabeth F.
Format: Artigo
Sprog:Inglês
Udgivet: National Academy of Sciences 1973
Fag:
Biological Sciences: Medical Sciences
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC433682/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4269173/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.70.7.2134
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