A method for α-L-iduronidase assay
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(74)80854-9/fullpdf
Reference12 articles.
1. L-iduronidase in cultured human fibroblasts and liver
2. Scheie and Hurler Syndromes: Apparent Identity of the Biochemical Defect
3. The Defect in the Hurler and Scheie Syndromes: Deficiency of -L-Iduronidase
4. The phenyl α- and β-L-idopyranosiduronic acids and some other aryl glycopyranosiduronic acids
5. α-L-iduronidase in lysosomal extracts
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1. α-L-iduronidase deficiency in mucopolysaccharidosis type I against a radio-labelled sulfated disaccharide substrate derived from dermatan sulfate;Clinical Genetics;2008-04-23
2. Medium effect on the reaction of gibb's reagent with sodium thiosulphate;Journal of Chemical Technology and Biotechnology. Chemical Technology;2007-05-29
3. Detection of Mucopolysaccharidosis Type I Heterozygotes Based on the Biochemical Characteristics of Leukocyte α-L-Iduronidase;Archives of Medical Research;2002-01
4. Detection of mucopolysaccharidosis type I heterozygotes on the basis of the biochemical properties of plasma α-l-iduronidase;Clinica Chimica Acta;2001-10
5. Diagnostic Enzymology of a-L-Iduronidase with Special Reference to a Sulphated Disaccharide Derived from Heparin;Clinical Science;1982-02-01
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