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Clarifying lysosomal storage diseases
Lysosomal storage diseases (LSDs) are a class of metabolic disorders caused by mutations in proteins critical for lysosomal function. Such proteins include lysosomal enzymes, lysosomal integral membrane proteins, and proteins involved in the post-translational modification and trafficking of lysosom...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2011
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3153126/ https://ncbi.nlm.nih.gov/pubmed/21723623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tins.2011.05.006 |
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