ENZYME DEFECTS OF GLYCOSAMINOGLYCAN DEGRADATION IN THE MUCOPOLYSACCHARIDOSES
- 1 August 1974
- journal article
- Published by Wiley in Developmental Medicine and Child Neurology
- Vol. 16 (4) , 534-539
- https://doi.org/10.1111/j.1469-8749.1974.tb03381.x
Abstract
No abstract availableThis publication has 37 references indexed in Scilit:
- IN-VITRO CONFIRMATION OF GENETIC COMPOUND OF THE HURLER AND SCHEIE SYNDROMESThe Lancet, 1974
- Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisThe Journal of Pediatrics, 1973
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- A Form of Mucopolysaccharidosis with Visceral Storage and Excessive Urinary Excretion of Chondroitin SulphateDevelopmental Medicine and Child Neurology, 1972
- A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)The Journal of Pediatrics, 1972
- Biochemical heterogeneity of the sanfilippo syndrome: Preliminary characterization of two deficient factorsBiochemical and Biophysical Research Communications, 1971
- L-iduronidase in cultured human fibroblasts and liverBiochemical and Biophysical Research Communications, 1971
- HURLER'S SYNDROMEThe Journal of Experimental Medicine, 1966
- Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type)The Journal of Pediatrics, 1963
- The uronic acid of heparinBiochemical and Biophysical Research Communications, 1962