Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblasts
- 24 July 1974
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 59 (2), 455-461
- https://doi.org/10.1016/s0006-291x(74)80001-x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)American Journal of Diseases of Children, 1973
- α-l-Iduronidase activity in cultured skin fibroblasts and amniotic fluid cellsArchives of Biochemistry and Biophysics, 1973
- Mucopolysaccharidosis: Secondarily Induced Abnormal Distribution of Lysosomal IsoenzymesScience, 1973
- A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)The Journal of Pediatrics, 1972
- THE GENETIC MUCOPOLYSACCHARIDOSESMedicine, 1965
- The assay of arylsulphatases A and B in human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1959