Degradation of keratan sulfate by ß-N-acetylhexosaminidases in GM2-gangliosidosis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb00963.x/fullpdf
Reference12 articles.
1. Defective glycosaminoglycans catabolism in cultured fibroblasts and its correction by N-acetylhexosaminidase;Cantz;Europ. J. Biochem.,1974
2. A new method for the desulfation of chondroitin sulfate;Kantor;J. Amer. chem, Soc.,1957
3. Beta-galactosidase deficient type mucolipidosis in somatic cell hybrids;Kato;Biochem. Biophs. Res. Commun.,1979
4. Degradation of keratan sulfate by β-N-acetylhexosaminidase;Ludolph;Biochem. J.,1981
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1. Mucopolysaccharidosis-like phenotype in feline Sandhoff disease and partial correction after AAV gene therapy;Molecular Genetics and Metabolism;2015-09
2. Impaired degradation of chondroitin sulfate in GM2-gangliosidosis;Clinical Genetics;2008-04-23
3. Glycosaminoglycan Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
4. Diagnosis of Tay-Sachs disease by estimation of β-N-acetylhexosaminidase activity using a radiolabeled hyaluronic acid-derived trisaccharide substrate;Clinica Chimica Acta;1984-02
5. Diagnosis of Tay—Sachs disease using radiolabelled chondroitin 6-sulphate-derived trisaccharides;Journal of Inherited Metabolic Disease;1983-06
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