Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study

Genetic testing for BRCA1 and BRCA2 is crucial in diagnosing hereditary breast and ovarian cancer syndromes and has increased with the development of multigene panel tests. However, results classified as variants of uncertain significance (VUS) present challenges to clinicians in attempting to choos...

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Detalles Bibliográficos
Autores principales: Kim, Joo Heung, Park, Sunggyun, Park, Hyung Seok, Park, Ji Soo, Lee, Seung-Tae, Kim, Sung-Won, Lee, Jong Won, Lee, Min Hyuk, Park, Sue K., Noh, Woo-Chul, Choi, Doo Ho, Han, Wonshik, Jung, Sung Hoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055990/
https://www.ncbi.nlm.nih.gov/pubmed/33875706
http://dx.doi.org/10.1038/s41598-021-87792-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055990/
https://www.ncbi.nlm.nih.gov/pubmed/33875706
http://dx.doi.org/10.1038/s41598-021-87792-w

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