Clinical management of breast cancer families is complicated by identification of BRCA1 and BRCA2 sequence alterations of unknown significance. Molecular assays evaluating the effect of intronic variants on native splicing can help determine their clinical relevance. Twentysix intronic BRCA1/2 varia
✦ LIBER ✦
Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study
✍ Scribed by Caux-Moncoutier, Virginie; Pagès-Berhouet, Sabine; Michaux, Dorothée; Asselain, Bernard; Castéra, Laurent; De Pauw, Antoine; Buecher, Bruno; Gauthier-Villars, Marion; Stoppa-Lyonnet, Dominique; Houdayer, Claude
- Book ID
- 109849186
- Publisher
- Nature Publishing Group
- Year
- 2009
- Tongue
- English
- Weight
- 181 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1018-4813
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We have examined the role of the breast cancer susceptibility genes BRCA1 and BRCA2 and other loci in the vicinity of these 2 genes on the long arms of chromosomes 17 and 13 (17q and 13q) for the presence of genomic deletions in breast cancer among Taiwanese women. Breast cancer in Taiwan is particu