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Ribosomal protein gene deletions in Diamond-Blackfan anemia
Diamond-Blackfan anemia (DBA) is a congenital BM failure syndrome characterized by hypoproliferative anemia, associated physical abnormalities, and a predisposition to cancer. Perturbations of the ribosome appear to be critically important in DBA; alterations in 9 different ribosomal protein genes h...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Hematology
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3245214/ https://ncbi.nlm.nih.gov/pubmed/22045982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2011-08-375170 |
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