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Characterization of Drosophila Saposin-related mutants as a model for lysosomal sphingolipid storage diseases
Sphingolipidoses are inherited diseases belonging to the class of lysosomal storage diseases (LSDs), which are characterized by the accumulation of indigestible material in the lysosome caused by specific defects in the lysosomal degradation machinery. While some LSDs can be efficiently treated by e...
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| 出版年: | Dis Model Mech |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Company of Biologists Ltd
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5483003/ https://ncbi.nlm.nih.gov/pubmed/28389479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.027953 |
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