The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation-Reference-Cited by-同舟云学术

The apolipoprotein C-III (Gln38Lys) variant associated with human hypertriglyceridemia is a gain-of-function mutation

Published:2017-11 Issue:11 Volume:58 Page:2188-2196
ISSN:0022-2275
Container-title:Journal of Lipid Research
language:en
Short-container-title:Journal of Lipid Research

Author:

Sundaram Meenakshi,Curtis Kaitlin R.,Amir Alipour Mohsen,LeBlond Nicholas D.,Margison Kaitlyn D.,Yaworski Rebecca A.,Parks Robin J.,McIntyre Adam D.,Hegele Robert A.,Fullerton Morgan D.,Yao Zemin

Funder

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Cell Biology,Endocrinology,Biochemistry

Reference33 articles.

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5. Loss-of-function mutations in APOC3 and risk of ischemic vascular disease;Jørgensen;N. Engl. J. Med.,2014

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