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SGSH gene

Known as: N-sulfoglucosamine sulfohydrolase, HEPARAN SULFATE SULFATASE, SGSH 
 
National Institutes of Health

Papers overview

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2016
2016
Mucopolysaccharidosis IIIA (MPS IIIA) is a neurodegenerative lysosomal storage disorder characterised by progressive loss of… Expand
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2015
2015
AIMS For the standardization of flow-mediated vasodilatation (FMD) assessment as a clinical tool, validation of its reliability… Expand
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2014
2014
Mucopolysaccharidosis type IIIA (Sanfilippo A syndrome), a fatal childhood-onset neurodegenerative disease with mild facial… Expand
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2012
2012
Mucopolysaccharidosis type IIIA (MPSIIIA) is an inherited lysosomal storage disease caused by deficiency of sulfamidase… Expand
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2009
2009
Mucopolysaccharidosis type IIIA (MPS IIIA) results from lack of functional sulfamidase (SGSH), a lysosomal enzyme. Its substrate… Expand
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2009
2009
The biosynthesis study of antibiotics saframycin (SFM) in Streptomyces lavendulae and safracin (SAC) in Pseudomonas fluorescens… Expand
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2008
2008
Mucopolysaccharidosis type IIIA (MPS IIIA), which is a lysosomal storage disorder (LSD) caused by inherited deficiency of… Expand
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2007
2007
At present, there is no widely available, safe and effective treatment for lysosomal storage disorders (LSD) that affect the… Expand
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2004
2004
Lysosomal storage disorders (LSD) are rare inherited metabolic diseases in which genetic alterations affect lysosomal proteins… Expand
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2004
2004
Mucopolysaccharidosis IIIA (MPS IIIA; Sanfilippo syndrome) is an autosomal recessive lysosomal disorder caused by the deficiency… Expand
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