A model of mucopolysaccharidosis IIIB (Sanfilippo syndrome type IIIB): N‐acetyl‐α‐D‐glucosaminidase deficiency in Schipperke dogs
- 1 July 2003
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 26 (5) , 489-504
- https://doi.org/10.1023/a:1025177411938
Abstract
Mucopolysaccharidosis III (MPS III) is characterized by lysosomal accumulation of the glycosaminoglycan (GAG) heparan sulphate (HS). In humans, the disease manifests in early childhood, and is...Keywords
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