Mucopolysaccharidosis type We (MPS I) is one of the most common lysosomal storage diseases with progressive neurological dysfunction. month aged when reduced visual cognitive memory retention was noted in the IDUA?/? mice. In addition, 8-month aged IDUA?/? mice failed to habituate to repeated open-field exposure, suggesting deficits in nonaversive and non-associative memory. In acoustic startle… Continue reading Mucopolysaccharidosis type We (MPS I) is one of the most common