Regional localization of α-galactosidase (GLA) to Xpter→q22, hexosaminidase B (HEXB) to 5q13→qter, and arylsulfatase B (ARSB) to 5pter→q13
- 1 January 1984
- journal article
- research article
- Published by S. Karger AG in Cytogenetic and Genome Research
- Vol. 38 (1), 45-49
- https://doi.org/10.1159/000132028
Abstract
Two series of somatic cell hybrids were made by fusion of human cells with karyotypes 46, X, t(X;2;15)(q22;p12;p12) and 46, XX, t(5;7)(q13;p15) and rodent cells. Chromosome and isozyme analysis of human chromosomes and gene products in the hybrids localized GLA to Xpter→q22, HEXB to 5q13→qter, in both cases narrowing the regional assignments, and ARSB to 5pter→q13.Keywords
This publication has 3 references indexed in Scilit:
- Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and BProceedings of the National Academy of Sciences, 1979
- Characterization of ?-galactosidase isoenzymes in normal and fabry human-Chinese hamster somatic cell hybridsHuman Genetics, 1977
- Enzymatic Defect in Fabry's DiseaseNew England Journal of Medicine, 1967