A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)
Authors:
- Robert W. BartonRBRobert W. Barton
- Elizabeth F. NeufeldENElizabeth F. Neufeld
- 31 January 1972
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 80 (1) , 114-116
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Inborn Errors of Mucopolysaccharide MetabolismScience, 1970
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- 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