Mannosidosis: Deficiency of a specific α-mannosidase component in cultured fibroblasts
- 22 February 1975
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 59 (1), 93-99
- https://doi.org/10.1016/0009-8981(75)90223-5
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Mannosidosis: Detection of the disease and of heterozygotes using serum and leucocytesBiochemical and Biophysical Research Communications, 1974
- Mucolipidosis III (Pseudo-Hurler Polydystrophy): Multiple Lysosomal Enzyme Abnormalities in Serum and Cultured Fibroblast CellsPediatric Research, 1973
- Mucolipidosis III (pseudo‐Hurler polydystrophy): Cytological and ultrastructural observations of cultured fibroblast cellsClinical Genetics, 1973
- Electrophoretic heterogeneity of human α-mannosidaseBiochimica et Biophysica Acta (BBA) - Protein Structure, 1973
- Human mannosidosis — The enzymic defectBiochemical and Biophysical Research Communications, 1972
- Properties of α-Mannosidase in MannosidosisScandinavian Journal of Clinical and Laboratory Investigation, 1970
- Mannosidosis: A clinical and histopathologic studyThe Journal of Pediatrics, 1969
- Mannosidosis: Isolation of oligosaccharide storage material from brainThe 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