Pub. Date : 2017 Mar
PMID : 28150116
4 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of alpha-L-iduronidase (IDUA), resulting in accumulation of glycosaminoglycans (GAG) in lysosomes. | Glycosaminoglycans | iduronidase, alpha-L | Mus musculus |
2 | Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of alpha-L-iduronidase (IDUA), resulting in accumulation of glycosaminoglycans (GAG) in lysosomes. | Glycosaminoglycans | iduronidase, alpha-L | Mus musculus |
3 | Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of alpha-L-iduronidase (IDUA), resulting in accumulation of glycosaminoglycans (GAG) in lysosomes. | Glycosaminoglycans | iduronidase, alpha-L | Mus musculus |
4 | Mucopolysaccharidosis type I (MPS I) is caused by a deficiency of alpha-L-iduronidase (IDUA), resulting in accumulation of glycosaminoglycans (GAG) in lysosomes. | Glycosaminoglycans | iduronidase, alpha-L | Mus musculus |