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BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study
BACKGROUND: Inactivating and truncating mutations of the nuclear BRCA1-interacting protein 1 (BRIP1) have been shown to be the major cause of Fanconi anaemia and, due to subsequent alterations of BRCA1 function, predispose to breast cancer (BC). METHODS: We investigated the effect of BRIP1 -64G>A...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1887536/ https://ncbi.nlm.nih.gov/pubmed/17504528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2407-7-83 |
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