GENETIC HETEROGENEITY IN LYSOSOMAL STORAGE DISORDERS STUDIED BY SOMATIC CELL HYBRIDIZATION
- 1 January 1984
- book chapter
- Published by Elsevier
Abstract
No abstract availableThis publication has 103 references indexed in Scilit:
- Purification of acid β-galactosidase and acid neuraminidase from bovine testis: Evidence for an enzyme complexBiochemical and Biophysical Research Communications, 1982
- Acute neuronopathic (infantile) and chronic nonneuronopathic (adult) Gaucher disease in full siblingsThe Journal of Pediatrics, 1982
- Correction of combined β-galactosidase/neuraminidase deficiency in human fibroblastsBiochemical and Biophysical Research Communications, 1981
- The complementation of β-galactosidase in fused cells of mucolipidosis II with another variants of β-galactosidase deficiency using new single cell enzyme assayBiochemical and Biophysical Research Communications, 1979
- Non-selective isolation of human somatic cell hybrids by unit-gravity sedimentationNature, 1979
- The enzymic defect in Morquio's disease: The specificity of N-acetylhexosamine sulfatasesBiochemical and Biophysical Research Communications, 1978
- Genetic heterogeneity in GM1-gangliosidosisNature, 1975
- Morquio's syndrome: Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfataseBiochemical and Biophysical Research Communications, 1974
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- Hybrid protein formation of E. coli alkaline phosphatase leading to in vitro complementationJournal of Molecular Biology, 1963