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Beneficial metabolic phenotypes caused by loss‐of‐function APOC3 mutations
Author(s) -
Gibson W. T.
Publication year - 2015
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12483
Subject(s) - loss function , phenotype , mutation , genetics , medicine , function (biology) , endocrinology , biology , gene
Loss‐of‐function mutations in APOC3 , triglycerides, and coronary disease. TG & HDL Working Group of the NHLBI Exome Sequencing Project (2014) N Engl J Med 371:22–31 Loss‐of‐function mutations in APOC3 and risk of ischemic vascular disease. Jørgensen et al. (2014) N Engl J Med 371:32–41
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