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Expression and Endocytosis of Lysosomal Aspartylglucosaminidase in Mouse Primary Neurons
Aspartylglucosaminuria (AGU) is a neurodegenerative lysosomal storage disease that is caused by mutations in the gene encoding for a soluble hydrolase, aspartylglucosaminidase (AGA). In this study, we have used our recently developed mouse model for AGU and analyzed processing, intracellular localiz...
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| 出版年: | J Neurosci |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Society for Neuroscience
1998
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6793022/ https://ncbi.nlm.nih.gov/pubmed/9742145 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.18-19-07750.1998 |
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