Enzyme replacement therapy for murine mucopolysaccharidosis type VII leads to improvements in behavior and auditory function.

Mucopolysaccharidosis type VII (MPS VII; Sly syndrome) is one of a group of lysosomal storage diseases that share many clinical features, including mental retardation and hearing loss. Lysosomal storage in neurons of the brain and the associated behavioral abnormalities characteristic of a murine mo...

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Hlavní autoři: O'Connor, L H, Erway, L C, Vogler, C A, Sly, W S, Nicholes, A, Grubb, J, Holmberg, S W, Levy, B, Sands, M S
Médium: Artigo
Jazyk:Inglês
Vydáno: 1998
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC508717/
https://ncbi.nlm.nih.gov/pubmed/9525982
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