Correction of combined β-galactosidase/neuraminidase deficiency in human fibroblasts
- 1 November 1981
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 103 (1), 292-300
- https://doi.org/10.1016/0006-291x(81)91692-2
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Atypical expression of ß-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalitiesClinical Genetics, 2008
- Complementation analysis of human sialidase deficiency using natural substratesAnnals of Human Genetics, 1981
- Genetic heterogeneity in human neuraminidase deficiencyNature, 1980
- Prenatal diagnosis of sialidosis with combined neuraminidase and ø‐galactosidase deficiencyClinical Genetics, 1979
- Adult type GMl-gangliosidosis: A complementation study on somatic cell hybridsBrain & Development, 1979
- Affinity labelling with a deaminatively generated carbonium ion. Kinetics and stoicheiometry of the alkylation of methionine-500 of the lacZ β-galactosidase of Escherichia coli by β-d-galactopyranosylmethyl-p-nitrophenyltriazeneBiochemical Journal, 1978
- Macular cherry-red spots and myoclonus with dementia: Coexistent neuraminidase and β-galactosidase deficienciesBiochemical and Biophysical Research Communications, 1978
- In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stainExperimental Cell Research, 1977
- Purification of human liver acid β-d-galactosidases using affinity chromatographyAnalytical Biochemistry, 1976
- Genetic heterogeneity in GM1-gangliosidosisNature, 1975