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Mucopolysaccharidosis IIIB (MPS IIIB) is an inherited metabolic disease due to deficiency of α-N-Acetylglucosaminidase (NAGLU) enzyme with subsequent storage of undegradedheparan sulfate (HS). The main clinical manifestations of the disease are profound intellectual disability and neurodegene...
ORGANISM(S): Mus musculus (Mouse) 
2020-02-26 | PXD017363 | Pride
A Drosophila model of mucopolysaccharidosis IIIB
Mucopolysaccharidosis IIIB (MPS IIIB) is a rare genetic disorder caused by defects in α-N-acetylglucosaminidase, which breaks down extracellular heparan sulfate. Symptoms progress from hyperactivity and sleep disruptions during childhood to severe neurodegeneration during adolescence. To generate an...
ORGANISM(S): Drosophila melanogaster 
2025-03-26 | GSE269032 | GEO
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