Title : Molecular analysis of mucopolysaccharidosis type I in Tunisia: identification of novel mutation and eight Novel polymorphisms.

Pub. Date : 2011 Apr 26

PMID : 21521498






2 Functional Relationships(s)
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Protein Name
Organism
1 UNLABELLED: Mucopolysaccharidosis type I (MPS I) is an autosomal recessive lysosomal storage disorder caused by a genetic defect in alpha-L-iduronidase (IDUA) which is involved in the degradation of dermatan and heparan sulfates. Dermatan Sulfate alpha-L-iduronidase Homo sapiens
2 UNLABELLED: Mucopolysaccharidosis type I (MPS I) is an autosomal recessive lysosomal storage disorder caused by a genetic defect in alpha-L-iduronidase (IDUA) which is involved in the degradation of dermatan and heparan sulfates. Dermatan Sulfate alpha-L-iduronidase Homo sapiens