A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.
Colorectal cancer (CRC) is a complex disease, and therefore its development is determined by the combination of both environmental factors and genetic variants. Although genome-wide association studies (GWAS) of SNP variation have conveniently identified 20 genetic variants so far, a significant pro...
Главные авторы: | , , , , , , , , , , , , , , , , , , , , , |
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Формат: | Journal article |
Язык: | English |
Опубликовано: |
2014
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