Abstract
Certain variants of apolipoprotein (apo) E, encoded by the APOE gene, have been associated with lipid disorders. Previously, there has been contradictory evidence regarding the association between the rare p.L46P substitution and dyslipidemia. The purpose of this study is to analyze the lipid profile of patients with the APOE c.T137C:p.L46P missense mutation to identify an association with a specific phenotype.
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