Title : Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients.

Pub. Date : 1996 Jun

PMID : 8651289






1 Functional Relationships(s)
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Protein Name
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1 Maroteaux-Lamy syndrome, or mucopolysaccharidosis type VI (MPS-VI), is a lysosomal storage disorder characterized by the defective degradation of dermatan sulfate due to the deficiency of N-acetylgalactosamine-4-sulfatase (4S). Dermatan Sulfate arylsulfatase B Homo sapiens