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N-acetylgalactosaminidase


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EC 3.2.1.53; either of two lysosomal enzymes that catalyse the hydrolysis of respectively α‐ and β‐linked terminal nonreducing N‐acetyl‐d‐galactosamine residues. Deficiency of α‐N‐acetylgalactosaminidase is associated with a storage disease (Schindler disease) in which sialyloligosaccharides are found in urine.

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Subjects: Chemistry.


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