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Mutation screening of germline TP53 mutations in high-risk Chinese breast cancer patients
BACKGROUND: Germline TP53 mutations are associated with Li-Fraumeni syndrome, a severe and rare hereditary cancer syndrome. Despite the rarity of germline TP53 mutations, the clinical implication for mutation carriers and their families is significant. The risk management of TP53 germline mutation c...
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| Publicado no: | BMC Cancer |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7607817/ https://ncbi.nlm.nih.gov/pubmed/33138793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-020-07476-y |
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