Prevalence of ANGPTL3 and APOB Gene Mutations in Subjects With Combined Hypolipidemia-Reference-Cited by-同舟云学术

Prevalence of ANGPTL3 and APOB Gene Mutations in Subjects With Combined Hypolipidemia

Published:2012-03 Issue:3 Volume:32 Page:805-809
ISSN:1079-5642
Container-title:Arteriosclerosis, Thrombosis, and Vascular Biology
language:en
Short-container-title:Arterioscler Thromb Vasc Biol.

Author:

Noto Davide¹,Cefalù Angelo B.¹,Valenti Vincenza¹,Fayer Francesca¹,Pinotti Elisa¹,Ditta Mariangela¹,Spina Rossella¹,Vigna Giovanni¹,Yue Pin¹,Kathiresan Sekar¹,Tarugi Patrizia¹,Averna Maurizio R.¹

Affiliation:

1. From the Department of Internal Medicine and Medical Specialties (D.N., A.B.C., V.V., F.F., M.D., R.S., M.R.A.), University of Palermo, Italy; Department of Biomedical Sciences (E.P., P.T.), University of Modena & Reggio Emilia, Italy; Department of Clinical and Experimental Medicine (G.V.), University of Ferrara, Ferrara, Italy; School of Medicine, Washington University, St. Louis, MO (P.Y.); Cardiovascular Research Center and Center for Human Genetic Research (S.K.), Massachusetts General...

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

Reference18 articles.

1. Lipid Disorders and Mutations in the APOB Gene

2. Familial hypobetalipoproteinemia: genetics and metabolism

3. Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia

4. Mutations in MTP gene in abeta- and hypobeta-lipoproteinemia

5. Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9

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