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 from...

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Detalles Bibliográficos
Autores principales: Yamazawa, Kazuki, Sugano, Kokichi, Tanakaya, Kohji, Inoue, Satomi, Murakami, Haruka, Nakashima, Moeko, Adachi, Masataka, Oki, Shinya, Makabe, Takeshi, Yamashita, Hiroshi, Ueki, Arisa, Sasaoka, Ayako, Nakashoji, Ayako, Kinoshita, Takayuki, Matsunaga, Tatsuo, Arai, Masami, Nakamura, Seigo, Miyata, Hiroaki, Ikegami, Masachika, Mano, Hiroyuki, Kohsaka, Shinji, Matsui, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
ORIGINAL ARTICLES
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323079/
https://www.ncbi.nlm.nih.gov/pubmed/37067535
http://dx.doi.org/10.1111/cas.15799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10323079/
https://www.ncbi.nlm.nih.gov/pubmed/37067535
http://dx.doi.org/10.1111/cas.15799

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