Title : Caprine mucopolysaccharidosis-IIID: clinical, biochemical, morphological and immunohistochemical characteristics.

Pub. Date : 1998 Feb

PMID : 9600207






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Both forms of caprine MPS IIID result from a nonsense mutation and consequent deficiency of lysosomal N-acetylglucosamine 6-sulfatase (G6S) activity and are associated with tissue storage and urinary excretion of heparan sulfate (HS). Heparitin Sulfate glucosamine (N-acetyl)-6-sulfatase Homo sapiens
2 Both forms of caprine MPS IIID result from a nonsense mutation and consequent deficiency of lysosomal N-acetylglucosamine 6-sulfatase (G6S) activity and are associated with tissue storage and urinary excretion of heparan sulfate (HS). Heparitin Sulfate glucosamine (N-acetyl)-6-sulfatase Homo sapiens