tailieunhanh - A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans

OA is a complex disease caused by environmental and genetic risk factors. The purpose of this study is to identify candidate copy number variations (CNVs) associated with OA. Methods: We performed a genome-wide association study of CNV to identify potential loci that confer susceptibility to or protection from OA. |

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