Laddar...
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...
Sparad:
| Huvudupphovsmän: | , , , |
|---|---|
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
1973
|
| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC433682/ https://ncbi.nlm.nih.gov/pubmed/4269173 |
| Taggar: |
Lägg till en tagg
Inga taggar, Lägg till första taggen!
|