Pub. Date : 2021 Feb
PMID : 33434858
2 Functional Relationships(s)Download |
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 |