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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 en:Circ Res
Autores principales: Assimes, Themistocles L., Quertermous, Thomas
Formato: Artigo
Lenguaje:Inglês
Publicado: 2014
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Acceso en línea: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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