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Whole-exome sequencing of BRCA-negative breast cancer patients and case–control analyses identify variants associated with breast cancer susceptibility
BACKGROUND: For the majority of individuals with early-onset or familial breast cancer referred for genetic testing, the genetic basis of their familial breast cancer remains unexplained. To identify novel germline variants associated with breast cancer predisposition, whole-exome sequencing (WES) w...
Autores principales: | Lee, Ning Yuan, Hum, Melissa, Amali, Aseervatham Anusha, Lim, Wei Kiat, Wong, Matthew, Myint, Matthew Khine, Tay, Ru Jin, Ong, Pei-Yi, Samol, Jens, Lim, Chia Wei, Ang, Peter, Tan, Min-Han, Lee, Soo-Chin, Lee, Ann S. G. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685974/ https://www.ncbi.nlm.nih.gov/pubmed/36424660 http://dx.doi.org/10.1186/s40246-022-00435-7 |
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