Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach-Reference-Cited by-同舟云学术

Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach

Published:2015-10 Issue:2 Volume:242 Page:618-624
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Minicocci Ilenia^ORCID,Prisco Cristina,Montali Anna^ORCID,Di Costanzo Alessia^ORCID,Ceci Fabrizio,Pigna Giovanni^ORCID,Arca Marcello

Funder

Ministero dell’Università, Ricerca Scientifica e Tecnologica (MURST)

La Sapienza University of Rome

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference43 articles.

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3. Genetically determined apo B levels and peak LDL density predict angiographic response to intensive lipid-lowering therapy;Zambon;J. Intern. Med.,2006

4. Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia;Brunzell;J. Lipid Res.,1983

5. Nomogram to diagnose familial combined hyperlipidemia on the basis of results of a 5-year follow-up study;Veerkamp;Circulation,2004

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