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Biallelic inactivation of REV7 is associated with Fanconi anemia
Fanconi anemia (FA) is a recessive genetic disease characterized by congenital abnormalities, chromosome instability, progressive bone marrow failure (BMF), and a strong predisposition to cancer. Twenty FA genes have been identified, and the FANC proteins they encode cooperate in a common pathway th...
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| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5004932/ https://ncbi.nlm.nih.gov/pubmed/27500492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI88010 |
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