Rare BRCA1 haplotypes including 3′UTR SNPs associated with breast cancer risk

Genetic markers identifying women at an increased risk of developing breast cancer exist, yet the majority of inherited risk remains elusive. While numerous BRCA1 coding sequence mutations are associated with breast cancer risk, BRCA1 mutations account for less then 5% of breast cancer risk. Since 3...

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Detalhes bibliográficos
Main Authors: Pelletier, Cory, Speed, William C, Paranjape, Trupti, Keane, Katie, Blitzblau, Rachel, Hollestelle, Antoinette, Safavi, Kyan, van den Ouweland, Ans, Zelterman, Daniel, Slack, Frank J, Kidd, Kenneth K, Weidhaas, Joanne B
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2011
Assuntos:
Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3048078/
https://ncbi.nlm.nih.gov/pubmed/21191178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/cc.10.1.14359
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