Mucopolysaccharidosis type VI: Structural and clinical implications of mutations in N-acetylgalactosamine-4-sulfatase
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference45 articles.
1. Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B
2. Structure of a human lysosomal sulfatase
3. Review: The immunochemical analysis of enzyme from mucopolysaccharidoses patients
4. Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein
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