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Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
INTRODUCTION: Mutations in known predisposition genes account for only about a third of all multiple-case breast cancer families. We hypothesized that germline mutations in FANCD2, BRIP1/BACH1, LMO4 and SFN may account for some of the unexplained multiple-case breast cancer families. METHODS: The fa...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1410737/ https://www.ncbi.nlm.nih.gov/pubmed/16280053 http://dx.doi.org/10.1186/bcr1336 |