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Literature summary for 3.10.1.1 extracted from

  • Gliddon, B.L.; Hopwood, J.J.
    Enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA mice (2004), Pediatr. Res., 56, 65-72.
    View publication on PubMed

Application

Application Comment Organism
medicine enzyme-replacement therapy from birth delays the development of behavior and learning problems in mucopolysaccharidosis type IIIA mice. Recombinant human sulfamidase administered to mucopolysaccharidosis type IIIA mice Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
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