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Impaired autophagy: The collateral damage of lysosomal storage disorders
Lysosomal storage disorders (LSDs), which number over fifty, are monogenically inherited and caused by mutations in genes encoding proteins that are involved in lysosomal function. Lack of the functional protein results in storage of a distinctive material within the lysosomes, which for years was t...
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| 出版年: | EBioMedicine |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Elsevier
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7753127/ https://ncbi.nlm.nih.gov/pubmed/33341443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ebiom.2020.103166 |
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