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Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
Germline coding variants have not been systematically investigated for pancreatic ductal adenocarcinoma (PDAC). Here we report an exome-wide investigation using the Illumina Human Exome Beadchip with 943 PDAC cases and 3908 controls in the Chinese population, followed by two independent replicate sa...
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| Publicat a: | Nat Commun |
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| Autors principals: | , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6134090/ https://ncbi.nlm.nih.gov/pubmed/30206226 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-06136-x |
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