Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years. (Maroteaux-Lamy syndrome, type B)
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference54 articles.
1. : Lysosomal enzymes, In (ed): Lysosomes. Amsterdam, North-Holland, 1972, pp 46-135
2. A distinct biochemical deficit in the maroteaux-lamy syndrome (mucopolysaccharidosis VI)
3. N-Acetylglucosamine-6-sulfate sulfatase from human urine.
4. The assay of arylsulphatases A and B in human urine
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