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Items: 4

1.
Sanfilippo syndrome type D: identification of the first mutation in the N-acetylglucosamine-6-sulphatase gene
C Beesley, D Burke, M Jackson, A Vellodi, B Winchester, E Young
J Med Genet. 2003 Mar; 40(3): 192–194. doi: 10.1136/jmg.40.3.192
PMCID:
PMC1735378
SummaryPDF–89K
2.
Human liver N-acetylglucosamine-6-sulphate sulphatase. Catalytic properties.
C Freeman, J J Hopwood
Biochem J. 1987 Sep 1; 246(2): 355–365. doi: 10.1042/bj2460355
PMCID:
PMC1148284
SummaryPage BrowsePDF–1.8M
3.
Human liver N-acetylglucosamine-6-sulphate sulphatase. Purification and characterization.
C Freeman, P R Clements, J J Hopwood
Biochem J. 1987 Sep 1; 246(2): 347–354. doi: 10.1042/bj2460347
PMCID:
PMC1148283
SummaryPage BrowsePDF–1.6M
4.
Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.
H Kresse, E Paschke, K von Figura, W Gilberg, W Fuchs
Proc Natl Acad Sci U S A. 1980 Nov; 77(11): 6822–6826. doi: 10.1073/pnas.77.11.6822
PMCID:
PMC350382
SummaryPage BrowsePDF–969K

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