The pathogenic role of the BRCA2 c. 7847C >T (p.Ser2616Phe) variant in breast and ovarian cancer predisposition
Substantial numbers of variants of unknown significance (VUSs) have been identified in BRCA1 / 2 through genetic testing, which poses a significant clinical challenge because the contribution of these VUSs to cancer predisposition has not yet been determined. Here, we report 10 Japanese patients fro...
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Veröffentlicht in: | Cancer science 2023-07, Vol.114 (7), p.2993-3002 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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