Intergenic complementation after fusion of fibroblasts from different patients with β-galactosidase deficiency
- 1 January 1979
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Enzymology
- Vol. 566 (1) , 72-79
- https://doi.org/10.1016/0005-2744(79)90250-x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Atypical expression of ß-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalitiesClinical Genetics, 2008
- In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stainExperimental Cell Research, 1977
- ?-Galactosidase deficiency in juvenile and adult patientsHuman Genetics, 1977
- Molecular genetics of GM1β‐galactosidaseClinical Genetics, 1975
- Genetic heterogeneity in GM1-gangliosidosisNature, 1975
- G1 Ganglioside β-Galactosidase APublished by Elsevier ,1974
- ANGIOKERATOMA CORPORIS DIFFUSUM AND LYSOSOMAL ENZYME DEFICIENCYThe Lancet, 1974
- A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Ganglioside GM1 β-galactosidase: Studies in human liver and brainArchives of Biochemistry and Biophysics, 1973
- Generalized Gangliosidosis: Beta-Galactosidase DeficiencyScience, 1968