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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7753127/ https://www.ncbi.nlm.nih.gov/pubmed/33341443 http://dx.doi.org/10.1016/j.ebiom.2020.103166 |