Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia-Reference-Cited by-同舟云学术

Rare genetic variants with large effect on triglycerides in subjects with a clinical diagnosis of familial vs nonfamilial hypertriglyceridemia

Published:2016-07 Issue:4 Volume:10 Page:790-797
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

De Castro-Orós Isabel,Civeira Fernando,Pueyo María Jesús,Mateo-Gallego Rocío,Bolado-Carrancio Alfonso,Lamíquiz-Moneo Itziar,Álvarez-Sala Luis,Fabiani Fernando,Cofán Montserrat,Cenarro Ana,Rodríguez-Rey José Carlos,Ros Emilio,Pocoví Miguel

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference30 articles.

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4. Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: a case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study;Hopkins;Circulation,2003

5. Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia;De Castro-Orós;Circ Cardiovasc Genet,2014

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