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Insights into Hunter syndrome from the structure of iduronate-2-sulfatase
Hunter syndrome is a rare but devastating childhood disease caused by mutations in the IDS gene encoding iduronate-2-sulfatase, a crucial enzyme in the lysosomal degradation pathway of dermatan sulfate and heparan sulfate. These complex glycosaminoglycans have important roles in cell adhesion, growt...
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| Gepubliceerd in: | Nat Commun |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5472762/ https://ncbi.nlm.nih.gov/pubmed/28593992 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncomms15786 |
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