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Personalized medicine with germline pathogenic variants: Importance of population‐ and region‐wide evidence
Rare germline pathogenic variants in cancer‐predisposing genes have a high impact and potential for clinical utility. In the last 30 years, based on evidence of cancer risk associated with germline pathogenic variants, several measures have been suggested for personalized medicine, including the dev...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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John Wiley and Sons Inc.
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551596/ https://www.ncbi.nlm.nih.gov/pubmed/37530079 http://dx.doi.org/10.1111/cas.15922 |