A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)
- 31 January 1972
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 80 (1), 114-116
- https://doi.org/10.1016/s0022-3476(72)80467-0
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Induced Degradation of Glycosaminoglycans in Hurler's and Hunter's Syndromes by Plasma InfusionProceedings of the National Academy of Sciences, 1971
- Inborn Errors of Mucopolysaccharide MetabolismScience, 1970
- Scheie and Hurler Syndromes: Apparent Identity of the Biochemical DefectScience, 1970
- Characterization of the factor deficient in the Hunter syndrome by polyacrylamide gel electrophoresisBiochemical and Biophysical Research Communications, 1970
- THE DEFECT IN HURLER AND HUNTER SYNDROMES, II. DEFICIENCY OF SPECIFIC FACTORS INVOLVED IN MUCOPOLYSACCHARIDE DEGRADATIONProceedings of the National Academy of Sciences, 1969