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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Detalles Bibliográficos
Publicado en:BMC Musculoskelet Disord
Main Authors: Moon, Sanghoon, Keam, Bhumsuk, Hwang, Mi Yeong, Lee, Young, Park, Suyeon, Oh, Ji Hee, Kim, Yeon-Jung, Lee, Heun-Sik, Kim, Nam Hee, Kim, Young Jin, Kim, Dong-Hyun, Han, Bok-Ghee, Kim, Bong-Jo, Lee, Juyoung
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2015
Assuntos:
Research Article
Acceso en liña: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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