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FANCD2 and DNA Damage
Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare human genetic disease featuring an extremely high incidence of cancer and many congenital defects. Among those studies, FA group D2 protein (FANCD2) has emerged as the focal p...
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| Опубликовано в: : | Int J Mol Sci |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
MDPI
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5578191/ https://ncbi.nlm.nih.gov/pubmed/28825622 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms18081804 |
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