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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Sci Rep
Autors principals: 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
Idioma:Inglês
Publicat: Nature Publishing Group UK 2021
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars