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Recurrent Germline BRCA2 Gene Mutation in Lithuanian Family
Approximately 10% of all breast cancer (BC) cases are familial and caused by inheritance of mutant BRCA1, BRCA2, or some other genes from the same DNA reparation pathway. Genetic counseling in families with cancer history is a powerful means for early cancer detection and active risk reduction throu...
Tallennettuna:
| Julkaisussa: | Medicina (Kaunas) |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7143304/ https://ncbi.nlm.nih.gov/pubmed/32164353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medicina56030119 |
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