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Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB
α-N-Acetylglucosaminidase deficiency (mucopolysaccharidosis IIIB, MPS IIIB) and α-l-iduronidase deficiency (MPS I) are heritable lysosomal storage diseases; neurodegeneration is prominent in MPS IIIB and in severe cases of MPS I. We have obtained morphologic and molecular evidence for the involvemen...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The National Academy of Sciences
2003
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC149931/ https://ncbi.nlm.nih.gov/pubmed/12576554 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.252784899 |
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