Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

Plasma triglyceride levels are heritable and are correlated with the risk of coronary heart disease. Sequencing of the protein-coding regions of the human genome (the exome) has the potential to identify rare mutations that have a large effect on phenotype.We sequenced the protein-coding regions of...

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Bibliographic Details
Main Authors:	Crosby, J, Peloso, G, Auer, P, Crosslin, DR, Stitziel, N, Lange, L, Lu, Y, Tang, Z, Zhang, H, Hindy, G, Masca, N, Stirrups, K, Kanoni, S, Do, R, Jun, G, Hu, Y, Kang, H, Xue, C, Goel, A, Farrall, M, Duga, S, Merlini, P, Asselta, R, Girelli, D, Olivieri, O
Format:	Journal article
Language:	English
Published:	2014

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

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