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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2011
2011
Mutational analysis of the IDUA gene was performed in a cohort of 102 European patients with mucopolysaccharidosis type I. A… (More)
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2008
2008
Mucopolysaccharidosis Type I, Hurler's Syndrome, is a lysosomal storage disorder that affects the brain. The missing enzyme… (More)
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2005
2005
Mucopolysaccharidosis type I is a lysosomal disease due to mutations in the IDUA gene, resulting in deficiency of alpha-L… (More)
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2002
2002
Purpose: Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disorder resulting from a deficiency of the lysosomal… (More)
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Highly Cited
1997
Highly Cited
1997
As a 40 i s h w o m a n genera l i n t e r n i s t feeKng the compet ing tugs of fantily and profess ion, I w a s de l ighted at… (More)
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1996
1996
Résumé This paper discusses the nature and role of First Nation Elders in Toronto urban community organizations. It presents the… (More)
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1994
1994
Achondroplasia is the most common type of genetic dwarfism. It is characterized by disproportionate short stature and other… (More)
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1993
1993
MANY NURSING FACILITIES t h r o u g h o u t t h e U n i t e d States p r o v i d e da i ly s u p p o r t s e rv i ces for i n c o… (More)
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1992
1992
In humans, a deficiency of the lysosomal hydrolase alpha-L-iduronidase (IDUA;EC 3.2.1.76) results in the lysosomal storage of the… (More)
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1992
1992
α-L-iduronidase (IDUA), which when deficient causes mucopolysaccharidosis type I, is located near the Huntington disease locus… (More)
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