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Ribosome defects in disorders of erythropoiesis
Over the past decade, genetic lesions that cause ribosome dysfunction have been identified in both congenital and acquired human disorders. These discoveries have established a new category of disorders, known as ribosomopathies, in which the primary pathophysiology is related to impaired ribosome f...
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2011
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3689295/ https://ncbi.nlm.nih.gov/pubmed/21279816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12185-011-0776-0 |
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