Mannosidosis: Detection of the disease and of heterozygotes using serum and leucocytes
- 23 January 1974
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 56 (2) , 296-303
- https://doi.org/10.1016/0006-291x(74)90841-9
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- MANNOSIDOSIS: CLINICAL, FINE‐STRUCTURAL AND BIOCHEMICAL FINDINGS IN THREE CASESActa Paediatrica, 1973
- α-l-Fucosidase and α-d-mannosidase activity in the white blood cells in the disease and carrier state of fucosidosisClinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- DIAGNOSIS OF MANNOSIDOSISThe Lancet, 1973
- Human mannosidosis — The enzymic defectBiochemical and Biophysical Research Communications, 1972
- Acid hydrolases in uncultured amniotic fluid cellsClinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- Tay-Sachs DiseaseNew England Journal of Medicine, 1970
- Mannosidosis: A clinical and histopathologic studyThe Journal of Pediatrics, 1969
- Fluorimetric estimation of 4-methyl-umbelliferyl-α-mannosidase activity in blood plasmaClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- A GENERALISED STORAGE DISORDER RESEMBLING HURLER'S SYNDROMEThe Lancet, 1967
- Separation and properties of β-galactosidase, β-glucosidase, β-glucuronidase and N-acetyl-β-glucosaminidase from rat kidneyBiochemical Journal, 1967