Article

Urine proteome uncover common mechanism between mucopolysaccharidosis type I and II

2023-12-14

Abstract excerpt

Mucopolysaccharidosis (MPS) type I and II are two types of rare lysosomal storage diseases, which lead to the accumulation of glycosaminoglycans due to the lack of the enzyme alpha-L-iduronidase (IDUA) and iduronate 2-sulfatase (IDS) respectively. There are some similar pathogenic mechanisms and clinical phenotypes but also some specific minute manifestations between these two subtypes. To better understand the si...

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Literature Corpus work: c5cb7bb4-71c7-5a9b-ae74-e97e8691d71d
DOI: 10.21203/rs.3.rs-3736233/v1

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