Sequence variation in the Fanconi anemia gene FAA
Fanconi anemia (FA) is a genetically heterogeneous autosomal recessive syndrome associated with chromosomal instability, hypersensitivity to DNA crosslinking agents, and predisposition to malignancy. The gene for FA complementation group A (FAA) recently has been cloned. The cDNA is predicted to enc...
Na minha lista:
| Publicado no: | Proc Natl Acad Sci U S A |
|---|---|
| Principais autores: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
1997
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC24261/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9371798/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.24.13051 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|