Associated Papers
Rare variant genetic landscape of familial chylomicronemia syndrome (FCS) in the United Kingdom.
Bashir B et al.
Genetics in Medicine Open, 2025
40919303 (PubMed )
Supplement: mmc1.pdf
Genetic variation in apolipoprotein A-V in hypertriglyceridemia.
Perera SD et al.
Current Opinion in Lipidology, 2024
The pathogenic mutations of APOA5 in Chinese patients with hyperlipidemic acute pancreatitis.
Liu Y et al.
Lipids in Health and Disease, 2024
Gene panel for Mendelian strokes.
Fang F et al.
Stroke and Vascular Neurology, 2020
32341005 (PubMed )
Supplement: svn-2020-000352supp003.pdf
Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis.
Jin JL et al.
Ebiomedicine, 2018
30420299 (PubMed )
Supplement: mmc1.pdf
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.P086710-4.xlsx › Other_APO_genes
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