The mucopolysaccharidoses: Biochemistry and clinical symptoms
- 1 August 1981
- journal article
- Published by Springer Nature in Journal of Molecular Medicine
- Vol. 59 (16) , 867-876
- https://doi.org/10.1007/bf01721920
Abstract
No abstract availableKeywords
This publication has 62 references indexed in Scilit:
- Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in l-cell fibroblastsBiochemical and Biophysical Research Communications, 1981
- CARDIAC PUNCTURE OF FETUS WITH HURLER'S DISEASE AVOIDING ABORTION OF UNAFFECTED CO-TWINThe Lancet, 1978
- The enzymic defect in Morquio's disease: The specificity of N-acetylhexosamine sulfatasesBiochemical and Biophysical Research Communications, 1978
- The desulphation of hexosamine sulphates by arylsulphatase B1Cellular and Molecular Life Sciences, 1976
- Surface heparan sulphate as a control element in eukariotic cells: A working modelJournal of Theoretical Biology, 1976
- Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfataseBiochemical and Biophysical Research Communications, 1974
- Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblastsBiochemical and Biophysical Research Communications, 1974
- Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisThe Journal of Pediatrics, 1973
- The Sanfilippo B corrective factor: A N-acetyl-α-D-glucosaminidaseBiochemical and Biophysical Research Communications, 1972
- L-iduronidase in cultured human fibroblasts and liverBiochemical and Biophysical Research Communications, 1971