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Fanconi anemia pathway as a prospective target for cancer intervention
Fanconi anemia (FA) is a recessive genetic disorder caused by biallelic mutations in at least one of 22 FA genes. Beyond its pathological presentation of bone marrow failure and congenital abnormalities, FA is associated with chromosomal abnormality and genomic instability, and thus represents a gen...
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| Publicado no: | Cell Biosci |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7075017/ https://ncbi.nlm.nih.gov/pubmed/32190289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13578-020-00401-7 |
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