Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome-Reference-Cited by-同舟云学术

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Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndrome

Published:1975-06 Issue:3 Volume:64 Page:955-962
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Fluharty Arvan L.,Stevens Richard L.,Fung David,Peak Shirley,Kihara Hayato

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference16 articles.

1. The Metabolic Basis of Inherited Diseases;Dorfman,1972

2. Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)

3. Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblasts

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1. Mucopolysaccharidosis VI diagnosis by laboratory methods;LaboratoriumsMedizin;2018-10-25

2. Long-Term Galsulfase Treatment Associated With Improved Survival of Patients With Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome);Journal of Inborn Errors of Metabolism and Screening;2018-01

3. Expert recommendations for the laboratory diagnosis of MPS VI;Molecular Genetics and Metabolism;2012-05

4. Sulphatase A: An Arylsulphatase and a Glycosulphatase;Ciba Foundation Symposium 72 - Sulphur in Biology;2008-05-30

5. Glycosaminoglycan Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22

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