Title : Structure and sequence of the human alpha-L-iduronidase gene.

Pub. Date : 1992 Aug

PMID : 1505961






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 In humans, a deficiency of the lysosomal hydrolase alpha-L-iduronidase (IDUA;EC 3.2.1.76) results in the lysosomal storage of the glycosaminoglycans heparan sulfate and dermatan sulfate, thereby causing the lysosomal storage disorder mucopolysaccharidosis type I. Dermatan Sulfate alpha-L-iduronidase Homo sapiens
2 In humans, a deficiency of the lysosomal hydrolase alpha-L-iduronidase (IDUA;EC 3.2.1.76) results in the lysosomal storage of the glycosaminoglycans heparan sulfate and dermatan sulfate, thereby causing the lysosomal storage disorder mucopolysaccharidosis type I. Dermatan Sulfate alpha-L-iduronidase Homo sapiens