Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial Hypercholesterolemia-Reference-Cited by-同舟云学术

Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial Hypercholesterolemia

Published:2018-10 Issue:10 Volume:34 Page:1316-1324
ISSN:0828-282X
Container-title:Canadian Journal of Cardiology
language:en
Short-container-title:Canadian Journal of Cardiology

Author:

Iacocca Michael A.,Wang Jian,Sarkar Samantha,Dron Jacqueline S.^ORCID,Lagace Thomas,McIntyre Adam D.,Lau Paulina,Robinson John F.,Yang Ping,Knoll Joan H.,Cao Henian,McPherson Ruth,Hegele Robert A.^ORCID

Funder

Jacob J. Wolfe Distinguished Medical Research Chair

Edith Schulich Vinet Research Chair in Human Genetics

Martha G. Blackburn Chair in Cardiovascular Research

Canadian Institutes of Health Research

Heart and Stroke Foundation of Ontario

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

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4. Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein;Garcia;Science,2001

5. Description of a large family with autosomal dominant hypercholesterolemia associated with the APOE p.Leu167del mutation;Marduel;Hum Mutat,2013

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