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GNS Polyclonal Antibody, 100ul Metabolic enzymes The protein encoded by this

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GNS Polyclonal Antibody, 100ul Metabolic enzymes The protein encoded by thisThe product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

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Description

The protein encoded by this gene belongs to the aldehyde dehydrogenase family

and downregulation of it may serve as a good biomarker for predicting patient outcomes

involved in the maintenance in the progenitor stage by promoting the cell cycle

Among its related pathways are Packaging Of Telomere Ends

is a lysosomal cysteine proteinase that may play an important role in corneal physiology

GNS Polyclonal Antibody, 100ul Metabolic enzymes The protein encoded by thisThe product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

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