The use of α-l-iduronidase activity determinations in leucocytes for the detection of hurler and scheie syndromes
- 16 April 1975
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 60 (2), 259-262
- https://doi.org/10.1016/0009-8981(75)90134-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- Beta-Galactosidase Deficiency in the Hurler SyndromeNew England Journal of Medicine, 1969
- The Abnormalities of Lysosomal Enzymes in MucopolysaccharidosesEuropean Journal of Biochemistry, 1968
- Acid hydrolases in skin and plasma in gargoylism. Deficiency of β-galactosidase in skinClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- Lysosomal Acid Hydrolases in the Liver in Gargoylism Deficiency of 4-methylumbelliferyl-β-galactosidaseScandinavian Journal of Clinical and Laboratory Investigation, 1968