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Pathomechanisms in Lysosomal Storage Disorders
Lysosomal diseases are inherited metabolic disorders caused by defects in a wide spectrum of lysosomal and a few non-lysosomal proteins. In most cases a single type of primary storage material is identified, which has been used to name and classify the disorders: hence the terms sphingolipidoses, ga...
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| 發表在: | Biochim Biophys Acta |
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| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2008
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4382014/ https://ncbi.nlm.nih.gov/pubmed/19111580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbamcr.2008.11.014 |
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