Molecular and functional characterization of familial chylomicronemia syndrome-Reference-Cited by-同舟云学术

Molecular and functional characterization of familial chylomicronemia syndrome

Published:2018-02 Issue: Volume:269 Page:272-278
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Teramoto Ryota^ORCID,Tada Hayato,Kawashiri Masa-aki,Nohara Atsushi,Nakahashi Takuya,Konno Tetsuo,Inazu Akihiro,Mabuchi Hiroshi,Yamagishi Masakazu,Hayashi Kenshi

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference32 articles.

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3. A Japanese patient with lipoprotein lipase deficiency homozygous for the Gly188Glu mutation prevalent worldwide;Yoshida;J. Atheroscler. Thromb.,2000

4. Remnant cholesterol as a causal risk factor for ischemic heart disease;Varbo;J. Am. Coll. Cardiol.,2013

5. Common variants associated with plasma triglycerides and risk for coronary artery disease;Do;Nat. Genet.,2013

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