A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease)
Author:
Affiliation:
1. Institute of Organic Chemistry; Moscow Russia
2. ; Department of Clinical Genetics; Erasmus University; Rotterdam The Netherlands
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1012763026526/fullpdf
Reference7 articles.
1. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase;Bach;Proc Natl Acad Sci,1973
2. Enzymatic diagnosis of the genetic mucopolysaccharide storage disorders;Hall;Methods Enzymol,1978
3. α-L-iduronidase, β-D-glucuronidase, and 2-sulfo-L-iduronate 2-sulfatase: preparation and characterisation of radioactive substrates from heparin;Hopwood;Carbohydr Res,1979
4. A centrifuged-column procedure for the measurement of ligand binding in beef heart F1;Penefsky;Methods Enzymol,1979
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