PRELIMINARY NOTE
Author:
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry
Link
https://www.degruyter.com/document/doi/10.1515/bchm2.1978.359.2.1811/pdf
Reference9 articles.
1. Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)
2. Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblasts
3. Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfatase
4. Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome
5. Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome
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4. Improved high-performance liquid chromatographic method for N-acetylgalactosamine-4-sulfate sulfatase (arylsulfatase B) activity determination using uridine diphosho-N-acetylgalactosamine-4-sulfate;Journal of Chromatography B: Biomedical Sciences and Applications;1997-08
5. REFERENCES TO THE ENZYME LIST;Enzyme Nomenclature;1992
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