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The Biological Clock and the Molecular Basis of Lysosomal Storage Diseases
The lysosomal storage disorders encompass nearly fifty diseases provoked by lack or deficiency of enzymes essential for the breakdown of complex molecules and hallmarked by accumulation in the lysosomes of metabolic residues. Histochemistry and cytochemistry studies evidenced patterns of circadian v...
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| Publié dans: | JIMD Rep |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Springer Berlin Heidelberg
2015
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4361918/ https://ncbi.nlm.nih.gov/pubmed/25583520 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2014_354 |
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