Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Can...
Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
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Publisher
London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Contents
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 choose an appropriate management plans. We...
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Full title
Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study
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TN_cdi_doaj_primary_oai_doaj_org_article_b5010b431758434caee1abe0f2f5c7e7
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b5010b431758434caee1abe0f2f5c7e7
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-021-87792-w
