Pub. Date : 2012 Sep
PMID : 22704483
1 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Mucopolysaccharidosis type II (MPS II), or Hunter syndrome, is a lysosomal storage disorder caused by a deficiency of iduronate-2-sulfatase (IDS) and is characterized by the accumulation of glycosaminoglycans (GAGs). | Glycosaminoglycans | iduronate 2-sulfatase | Mus musculus |