Human alpha-N-acetylgalactosaminidase-molecular cloning, nucleotide sequence, and expression of a full-length cDNA. Homology with human alpha-galactosidase A suggests evolution from a common ancestral gene.
Open Access
- 1 December 1990
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 265 (35) , 21859-21866
- https://doi.org/10.1016/s0021-9258(18)45818-8
Abstract
No abstract availableThis publication has 36 references indexed in Scilit:
- Molecular cloning of a full-length cDNA for human α-N-acetylgalactosaminidase (α-galactosidase B)Biochemical and Biophysical Research Communications, 1989
- Neuroaxonal Dystrophy Due to Lysosomal α-N-Acetylgalactosaminidase DeficiencyNew England Journal of Medicine, 1989
- Polymerase-specific differences in the DNA intermediates of frameshift mutagenesisJournal of Molecular Biology, 1989
- Site-directed mutagenesis by overlap extension using the polymerase chain reactionGene, 1989
- α-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorderJournal of Inherited Metabolic Disease, 1988
- The role of the mammalian branchpoint sequence in pre-mRNA splicing.Genes & Development, 1988
- Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencingJournal of Molecular Biology, 1980
- The identification of α-galactosidase B from human liver as an α-acetylgalactosaminidaseBiochemical and Biophysical Research Communications, 1977
- Alpha-N-acetylgalactosaminidase: Isolation, properties and distribution of the human enzymeBiochemical Medicine, 1973
- Genetic heterogeneity of α‐galactosidase in fabry's diseaseFEBS Letters, 1972