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Study of Exonic Variation Identifies Incremental Information Regarding Lipid-Related and Coronary Heart Disease Genes
Recently, a modest-sized population-based study of exonic variants facilitated the identification of the causal gene, TM6SF2, in a gene-rich locus on 19p1 previously associated with cholesterol levels in blood. The study also provided compelling functional validation of the locus and evidence at the...
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| Publicado no: | Circ Res |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5316237/ https://ncbi.nlm.nih.gov/pubmed/25124323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.114.304693 |
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