Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia-Reference-Cited by-同舟云学术

Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia

Published:2019-11 Issue:11 Volume:60 Page:1953-1958
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Dron Jacqueline S.^ORCID,Wang Jian,McIntyre Adam D.,Cao Henian,Robinson John F.,Duell P. Barton,Manjoo Priya,Feng James,Movsesyan Irina,Malloy Mary J.,Pullinger Clive R.,Kane John P.,Hegele Robert A.^ORCID

Funder

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference37 articles.

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5. An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia;Johansen;Arterioscler. Thromb. Vasc. Biol.,2011

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