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A Case Study on PPM1D and 9 Other Shared Germline Alterations in a Family
BACKGROUND: The use of high-throughput genotyping techniques has enabled us to identify the rare germline genetic variants with different pathogenicity and penetrance, and understand their role in cancer predisposition. We report here a familial cancer case, a study from Western Indian. METHODS: NGS...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
West Asia Organization for Cancer Prevention
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505862/ https://www.ncbi.nlm.nih.gov/pubmed/37378944 http://dx.doi.org/10.31557/APJCP.2023.24.6.2129 |