Mucopolysaccharidosis type VII (β‐glucuronidase deficiency): a report of a new case and a survey of those in the literature
- 1 June 1982
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 21 (6) , 366-373
- https://doi.org/10.1111/j.1399-0004.1982.tb01389.x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Comprehensive urinary screening for inborn errors of complex carbohydrate metabolismKlinische Wochenschrift, 1979
- Chondroitin 4- and 6-Sulfaturia: A New Type of Inborn Error of Metabolism ?The Tohoku Journal of Experimental Medicine, 1979
- Variation in the phenotypic expression of β-glucuronidase deficiencyThe Journal of Pediatrics, 1975
- Mucopolysaccharidosis VII: ?-Glucuronidase deficiencyHuman Genetics, 1974
- A β-glucuronidase deficiency mucopolysaccharidosis: studies in cultured fibroblastsArchives of Biochemistry and Biophysics, 1973
- Beta glucuronidase deficiency: Report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosisThe Journal of Pediatrics, 1973
- [121] Corrective factors for inborn errors of mucopolysaccharide metabolismPublished by Elsevier ,1972
- Analytical and preparative separation of acidic glycosaminoglycans by electrophoresis in barium acetateAnalytical Biochemistry, 1968
- OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROMEProceedings of the National Academy of Sciences, 1957