Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00281065.pdf
Reference26 articles.
1. Archer IM, Harper PS, Wusteman FS (1982) Multiple forms of iduronate 2-sulphate sulphatase in human tissues and body fluids. Biochim Biophys Acta 708:134?140
2. Bach G, Eisenberg F Jr, Cantz M, Neufeld EF (1973) The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci USA 70:2134?2138
3. Bell CE, Sly WS, Brot FE (1977) Human ?-glucuronidase deficiency mucopolysaccharidosis. Identification of cross-reactive antigen in cultured fibroblasts of deficient patients by enzyme immunoassay. J Clin Invest 59:97?105
4. Di Natale P, Daniele A (1985) Iduronate sulfatase from human placenta. Biochim Biophys Acta 839:258?261
5. Di Natale P, Ronsisvalle L (1981) Identification and partial characterization of two enzyme forms of iduronate sulfatase from human placenta. Biochim Biophys Acta 661:106?111
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