Comparison of two low-density lipoprotein apheresis systems in patients with homozygous familial hypercholesterolemia
Author:
Affiliation:
1. Institute of Nutrition and Functional Foods, Laval University; Quebec City Québec Canada
2. Lipid Research Centre, Centre Hospitalier Universitaire de Québec Research Centre; Québec City Québec Canada
Funder
Natural Sciences and Engineering Research Council of Canada, Kaneka Pharma LLC (Osaka, Japan)
Publisher
Wiley
Subject
Hematology,General Medicine
Reference46 articles.
1. Proprotein convertase subtilisin kexin 9: the third locus implicated in autosomal dominant hypercholesterolemia;Maxwell;Curr Opin Lipidol,2005
2. Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians;Couture;Hum Mutat,1998
3. Identification of two novel LDL receptor gene defects in French-Canadian pediatric population: mutational analysis and biochemical studies;Assouline;Hum Mutat,1997
4. Deletion in the gene for the low-density-lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia;Hobbs;N Engl J Med,1987
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