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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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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | 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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