There is strong evidence that overtly inactivating mutations in RAD51C predispose to hereditary breast and ovarian cancer but the prevalence of such mutations, and whether they are associated with a particular clinical phenotype, remains unclear. Resolving these questions has important implications
โฆ LIBER โฆ
ScreeningRAD51Cnucleotide alterations in patients with a family history of breast and ovarian cancer
โ Scribed by Yonglan Zheng; Jing Zhang; Kisha Hope; Qun Niu; Dezheng Huo; Olufunmilayo I. Olopade
- Publisher
- Springer US
- Year
- 2010
- Tongue
- English
- Weight
- 270 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0167-6806
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