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A novel BRCA2 mutation in prostate cancer sensitive to combined radiotherapy and androgen deprivation therapy
Genetic factors contribute to more than 40% of prostate cancer risk, and mutations in BRCA1 and BRCA2 are well-established risk factors. By using target capture-based deep sequencing to identify potential pathogenic germline mutations, followed by Sanger sequencing to determine the loci of the mutat...
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| Publicado no: | Cancer Biol Ther |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6067857/ https://ncbi.nlm.nih.gov/pubmed/29580149 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384047.2018.1451278 |
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