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Biochemistry of glycosphingolipid storage disorders: implications for therapeutic intervention.
The physiological importance of the degradative processes in lysosomes is revealed by the existence of at least 40 distinct inherited diseases, the so-called lysosomal storage disorders. Most of these diseases are caused by a deficiency in a single lysosomal enzyme, or essential cofactor, and result...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2003
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1693181/ https://ncbi.nlm.nih.gov/pubmed/12803924 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2003.1273 |
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