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Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.

Skin fibroblasts from two patients who had symptoms of the Sanfilippo syndrome (mucopolysaccharidosis III) accumulated excessive amounts of heparan sulfate and were unable to release sulfate from N-acetylglucosamine-6-sulfate linkages in heparan sulfate-derived oligosaccharides. Keratan sulfate-deri...

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Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Principais autores: Kresse, H, Paschke, E, von Figura, K, Gilberg, W, Fuchs, W
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 1980
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC350382/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6450420/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.77.11.6822
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