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Mitochondria-associated ER membranes (MAMs) and lysosomal storage diseases
Lysosomal storage diseases (LSDs) comprise a large group of disorders of catabolism, mostly due to deficiency of a single glycan-cleaving hydrolase. The consequent endo-lysosomal accumulation of undigested or partially digested substrates in cells of virtually all organs, including the nervous syste...
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| Publicado en: | Cell Death Dis |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Nature Publishing Group UK
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5832421/ https://ncbi.nlm.nih.gov/pubmed/29491402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41419-017-0025-4 |
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