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IDUA gene

Known as: IDURONIDASE, ALPHA-L, IDUA, ALPHA-L-IDURONIDASE 
This gene plays a role in glycosaminoglycan metabolism.
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
A mouse model of mucopolysaccharidosis (MPS) type I, which is null for the lysosomal enzyme, α-L-iduronidase (IDUA), is treated… 
Highly Cited
2008
Highly Cited
2008
Mucopolysaccharidosis Type I, Hurler's Syndrome, is a lysosomal storage disorder that affects the brain. The missing enzyme, α‐L… 
Highly Cited
2005
Highly Cited
2005
Mucopolysaccharidosis type I is a lysosomal disease due to mutations in the IDUA gene, resulting in deficiency of alpha-L… 
1999
1999
Mucopolysaccharidosis Type I (MPS I) is the lysosomal storage disease caused by the deficient activity of alpha-L-iduronidase… 
1998
1998
This paper, using a multivariate VAR-GARCH analysis, examines the role of the UK stock market in the price behaviour of the ten… 
1996
1996
Choropleth maps are frequently used to analyse spatial variations in the risk of a disease. In such maps the relative risk is… 
Highly Cited
1994
Highly Cited
1994
Achondroplasia is the most common type of genetic dwarfism. It is characterized by disproportionate short stature and other…