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Author Title Type [ Year
] Filters: Author is Auer, Paul L and Keyword is Mutation [Clear All Filters]
Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N Engl J Med. 2014 ;371(1):22-31.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature. 2015 ;518(7537):102-6.