Exon splicing analysis of intronic variants in multigene cancer panel testing for hereditary breast/ovarian cancer

The use of multigene panel testing for patients with a predisposition to breast/ovarian cancer is increasing as the identification of variants is useful for diagnosis and disease management. We identified pathogenic and likely pathogenic (P/LP) variants of high‐and moderate‐risk genes using a 23‐gen...

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Dades bibliogràfiques
Publicat a:Cancer Sci
Autors principals: Ryu, Jin‐Sun, Lee, Hye‐Young, Cho, Eun Hae, Yoon, Kyong‐Ah, Kim, Min‐Kyeong, Joo, Jungnam, Lee, Eun‐Sook, Kang, Han‐Sung, Lee, Seeyoun, Lee, Dong Ock, Lim, Myong Cheol, Kong, Sun‐Young
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2020
Matèries:
Genetics, Genomics, and Proteomics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7540976/
https://ncbi.nlm.nih.gov/pubmed/32761968
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cas.14600
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