Title : Biomechanical and histological characterization of MPS I mice femurs.

Pub. Date : 2021 Feb

PMID : 33434858






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder characterized by alpha-L-iduronidase (IDUA) deficiency, an enzyme responsible for glycosaminoglycan degradation. Glycosaminoglycans iduronidase, alpha-L Mus musculus
2 Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder characterized by alpha-L-iduronidase (IDUA) deficiency, an enzyme responsible for glycosaminoglycan degradation. Glycosaminoglycans iduronidase, alpha-L Mus musculus