GLYCOSIDASES IN SKIN AND PLASMA IN HUNTER'S SYNDROME Abnormality of a β‐galactosidase in Skin
- 1 July 1968
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 57 (4), 281-284
- https://doi.org/10.1111/j.1651-2227.1968.tb07292.x
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Deficiency of β‐galactosidase and α‐mannosidase – Primary Enzyme Defects in Gargoylism and a New Generalized Disease?Acta Paediatrica, 1967
- Diagnosis of Hurler's syndrome in the hospital laboratory and the determination of its genetic type.Archives of Disease in Childhood, 1966
- THE GENETIC MUCOPOLYSACCHARIDOSESMedicine, 1965
- Hurler's disease, Morquio's disease, and related mucopolysaccharidosesThe Journal of Pediatrics, 1965
- Distinction Among Four Forms of Hurler's Syndrome.Experimental Biology and Medicine, 1964