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The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70
Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome that exhibits an erythroid-specific phenotype. In at least 70% of cases, DBA is related to a haploinsufficient germ line mutation in a ribosomal protein (RP) gene. Additional cases have been associated with mutations in...
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| Vydáno v: | Blood Adv |
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| Hlavní autoři: | , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society of Hematology
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5728147/ https://ncbi.nlm.nih.gov/pubmed/29296843 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017008078 |
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