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BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population
The association of BRCA1/2 mutations with melanoma is not completely determined; the interpretation of variants of unknown significance is also problematic. To evaluate these issues we explored the molecular basis of melanoma risk by performing whole-exome sequencing on a cohort of 96 unrelated Poli...
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| Izdano u: | PLoS One |
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| Glavni autori: | , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Public Library of Science
2018
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6171837/ https://ncbi.nlm.nih.gov/pubmed/30286154 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0204768 |
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