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The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region

BACKGROUND: Recent genome-wide association studies (GWAS) have shown that single nucleotide polymorphisms (SNPs) in the Chr9p21 region are associated with coronary artery disease (CAD). Most of the SNPs identified in this region are non-coding SNPs, suggesting that they may influence gene expression...

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Bibliografische gegevens
Gepubliceerd in:BMC Med Genomics
Hoofdauteurs: Zhao, Wei, Smith, Jennifer A, Mao, Guangmei, Fornage, Myriam, Peyser, Patricia A, Sun, Yan V, Turner, Stephen T, Kardia, Sharon LR
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BioMed Central 2015
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4432789/
https://ncbi.nlm.nih.gov/pubmed/25958224
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-015-0094-0
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