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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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Gepubliceerd in: | BMC Med Genomics |
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Hoofdauteurs: | , , , , , , , |
Formaat: | Artigo |
Taal: | Inglês |
Gepubliceerd in: |
BioMed Central
2015
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Onderwerpen: | |
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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