Glycan profiling of urine, amniotic fluid and ascitic fluid from galactosialidosis patients reveals novel oligosaccharides with reducing end hexose and aldohexonic acid residues
Author:
Publisher
Wiley
Subject
Cell Biology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1742-4658.2010.07707.x/fullpdf
Reference46 articles.
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2. Molecular defect in combined β-galactosidase and neuraminidase deficiency in man;D’Azzo;Proc Natl Acad Sci USA,1982
3. Association of N-acetylgalactosamine-6-sulfate sulfatase with the multienzyme lysosomal complex of β-galactosidase, cathepsin A, and neuraminidase. Possible implication for intralysosomal catabolism of keratan sulfate;Pshezhetsky;J Biol Chem,1996
4. Lysosomal multienzyme complex: biochemistry, genetics, and molecular pathophysiology;Pshezhetsky;Prog Nucleic Acid Res Mol Biol,2001
5. Sialidosis: a review of human neuraminidase deficiency;Lowden;Am J Hum Genet,1979
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