Associated Papers
Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.
Zhou Y et al.
Journal of Lipid Research, 2018
30076208 (PubMed )
Supplement: 10.1194_P086710_jlr.P086710-2.xlsx › GLGC
SNPs at the APOA5 gene account for the strong association with hypertriglyceridaemia at the APOA5/A4/C3/A1 locus on chromosome 11q23 in the Northern Irish population.
Wright WT et al.
Atherosclerosis, 2006
Apolipoprotein A-V: a potential modulator of plasma triglyceride levels in Turks.
Hodoglugil U et al.
Journal of Lipid Research, 2006
Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia.
Eichenbaum-Voline S et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 2004
Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels.
Pennacchio LA et al.
Human Molecular Genetics, 2002
Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.
Cefalù AB et al.
Journal of Clinical Lipidology, 0
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