GENETIC HETEROGENEITY OF GAUCHER'S DISEASE
- 1 January 1984
- book chapter
- Published by Elsevier
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Assignment of the gene coding for human β-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodiesHuman Genetics, 1983
- Monoclonal Antibodies against Human β‐GlucocerebrosidaseEuropean Journal of Biochemistry, 1983
- Biochemical Studies in a Patient with Subacute Neuropathic Gaucher Disease without Visceral Glucosylceramide StoragePediatric Research, 1983
- Enzymic Differentiation of Neurologic and Nonneurologic Forms of Gaucher's DiseaseJournal of Neuropathology and Experimental Neurology, 1982
- Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.Proceedings of the National Academy of Sciences, 1982
- beta-Glucosidase assays in the diagnosis of Gaucher's disease.Clinical Chemistry, 1982
- Inborn Lysosomal DiseasesGastroenterology, 1965
- Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's diseaseBiochemical and Biophysical Research Communications, 1965