A homozygous missense arginine to histidine substitution at position 482 of the ?-galactosidase in an Italian infantile GM1-gangliosidosis patient
- 1 November 1992
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 90 (3) , 247-250
- https://doi.org/10.1007/bf00220071
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients.1991
- Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases.1991
- Progressive inactivation of the expression of an erythroid transcriptional factor in GM- and G-CSF-dependent myeloid cell linesNucleic Acids Research, 1990
- ALTERNATIVE SPLICING OF BETA-GALACTOSIDASE MESSENGER-RNA GENERATES THE CLASSIC LYSOSOMAL-ENZYME AND A BETA-GALACTOSIDASE-RELATED PROTEIN1989
- Cloning, sequencing, and expression of cDNA for human β-galactosidaseBiochemical and Biophysical Research Communications, 1988
- Glycolipid and Glycoprotein DegradationPublished by Wiley ,1987
- The complete sequence of a full length cDNA for human liver glyceraldehyde-3-phosphate dehydrogenase: evidence for multiple mRNA speciesNucleic Acids Research, 1984
- MORQUIO SYNDROME (MUCOPOLYSACCHARIDOSIS-IV-B) ASSOCIATED WITH BETA-GALACTOSIDASE DEFICIENCY - REPORT OF 2 CASES1980
- Generalized Gangliosidosis: Beta-Galactosidase DeficiencyScience, 1968