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Congenital dyserythropoietic anemias: III's a charm
In this issue of Blood, Liljeholm et al show that congenital dyserythropoietic anemia (CDA) type III is caused by a missense mutation in KIF23, which encodes a ubiquitous protein that regulates daughter cell separation during mitosis.(1)
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| Main Authors: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society of Hematology
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3674662/ https://ncbi.nlm.nih.gov/pubmed/23744492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-05-497602 |
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