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Paper Details

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
N Engl J Med
516
2010
ANGPTL3, ANGPTL3 mutations, HDL cholesterol, Human, LDL cholesterol, angiopoietin-like 3 protein, cholesterol, combined hypolipidemia, endothelial lipase, exome, familial combined hypolipidemia, genome, high-density lipoprotein (HDL) cholesterol, humans, inherited disorders, lipoprotein lipase, low-density lipoprotein (LDL) cholesterol, participants, protein-coding regions, triglyceride, triglycerides
Author NameAffiliation
Kiran MusunuruCardiovascular Research Center, Massachusetts General Hospital, Boston University School of Public Health
Kiran MusunuruCardiovascular Research Center, Massachusetts General Hospital, Boston University School of Public Health
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Datasets

Release 1.2