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FANCC suppresses short telomere-initiated telomere sister chromatid exchange
Telomere shortening has been linked to rare human disorders that present with bone marrow failure including Fanconi anemia (FA). FANCC is one of the most commonly mutated FA genes in FA patients and the FANCC subtype tends to have a relatively early onset of bone marrow failure and hematologic malig...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2816614/ https://ncbi.nlm.nih.gov/pubmed/20022886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp556 |
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