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The Relationship of Mutation Carriage of BRCA1/2 and Family History in Triple-Negative Breast Cancer: Experience from a Diagnostic Center in Turkey.

Neslihan Düzkale TekerOlcay Kandemir
Published in: European journal of breast health (2021)
In cases with a diagnosis of TNBC, a significant relationship exists between the number of relatives with cancer in the family history and the risk of carrying mutations in the BRCA1/2 genes. This relationship can be confirmed further by large-scale studies with more cases.
Keyphrases
  • papillary thyroid
  • genome wide
  • gene expression
  • young adults
  • breast cancer risk
  • transcription factor
  • genome wide identification