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A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans
BACKGROUND: 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 susceptibilit...
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| Udgivet i: | BMC Musculoskelet Disord |
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| Main Authors: | , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4395893/ https://ncbi.nlm.nih.gov/pubmed/25880085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12891-015-0531-4 |
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