Characterization of the mutant N-acetylglucosaminylphosphotransferase in I-cell disease and pseudo-Hurler polydystrophy: complementation analysis and kinetic studies. [electronic resource]
Producer: 19861003Description: 106-16 p. digitalISSN:- 0013-9432
- Cells, Cultured
- Fibroblasts -- enzymology
- Glycoside Hydrolases -- metabolism
- Golgi Apparatus -- enzymology
- Humans
- Hybrid Cells -- enzymology
- Kinetics
- Methylmannosides
- Mucolipidoses -- enzymology
- Mutation
- Phosphotransferases -- genetics
- Skin -- enzymology
- Transferases (Other Substituted Phosphate Groups)
- Uridine Diphosphate N-Acetylglucosamine
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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