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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Bibliografske podrobnosti
izdano v:Sci Rep
Main Authors: 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
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group UK 2021
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8055990/
https://ncbi.nlm.nih.gov/pubmed/33875706
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-021-87792-w
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