Characterizing familial chylomicronemia syndrome: Baseline data of the APPROACH study

Author:

Blom Dirk J.,O'Dea Louis,Digenio Andres,Alexander Veronica J.,Karwatowska-Prokopczuk Ewa,Williams Karren R.,Hemphill Linda,Muñiz-Grijalvo Ovidio,Santos Raul D.,Baum Seth,Witztum Joseph L.

Publisher

Elsevier BV

Subject

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

Reference53 articles.

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2. Familial lipoprotein lipase deficiency;Burnett,1993

3. A system for phenotyping hyperlipoproteinemia;Fredrickson;Circulation,1965

4. Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia;Surendran;J Intern Med,2012

5. Spectrum of mutations of the LPL gene identified in Italy in patients with severe hypertriglyceridemia;Rabacchi;Atherosclerosis,2015

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