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Fetal origins of hematopoietic failure in a murine model of Fanconi anemia
Hematopoietic failure is the predominant clinical manifestation of Fanconi anemia (FA), a rare, recessively inherited disorder. Mutations in 1 of 15 genes that coordinately function in a complex pathway to maintain DNA integrity also predispose patients to constitutional defects in growth and develo...
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| Huvudupphovsmän: | , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
American Society of Hematology
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3645055/ https://ncbi.nlm.nih.gov/pubmed/23315168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2012-06-439679 |
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