Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiency
- 1 October 1999
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1455 (2-3) , 69-84
- https://doi.org/10.1016/s0925-4439(99)00077-0
Abstract
No abstract availableKeywords
This publication has 136 references indexed in Scilit:
- Human Lysosomal Alpha-mannosidase: Isolation and Nucleotide Sequence of the Full-Length cDNA: Volume200,Number 1 (1994), pages 239–245:Biochemical and Biophysical Research Communications, 1997
- Alpha-N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosisThe Journal of Pediatrics, 1994
- Human Lysosomal Alpha-Mannosidase: Isolation and Nucleotide Sequence of the Full-Length cDNABiochemical and Biophysical Research Communications, 1994
- A study of the heterogenous structure of guinea pig lysosomal β-mannosidase using a polyclonal antibodyBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1991
- Bovine β-mannosidase deficiencyBiochemical and Biophysical Research Communications, 1990
- Human α-L-fucosidase: Complete coding sequence form cDNA clonesBiochemical and Biophysical Research Communications, 1989
- Human β-Mannosidase DeficiencyNew England Journal of Medicine, 1986
- Synthesis of lysosomal α-mannosidase in normal and mannosidosis fibroblastsBiochemical and Biophysical Research Communications, 1983
- Mannosidosis: A clinical and histopathologic studyThe Journal of Pediatrics, 1969
- Mannosidosis: Isolation of oligosaccharide storage material from brainThe Journal of Pediatrics, 1969