A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug-Reference-Cited by-同舟云学术

A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug

Published:2019-01-03 Issue:1 Volume:19 Page:
ISSN:1471-2261
Container-title:BMC Cardiovascular Disorders
language:en
Short-container-title:BMC Cardiovasc Disord

Author:

Bogari Neda M.,Aljohani Ashwag,Amin Amr A.,Al-Allaf Faisal A.,Dannoun Anas,Taher Mohiuddin M.,Elsayed Atalla,Rednah Dareen ibrahim,Elkhatee Osama,Porqueddu Massimo,Alamanni Francesco,Khogeer Soud Abdulraof A.,Fawzy Ahmed^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12872-018-0965-3.pdf

Reference21 articles.

1. Ding Y, et al. Associations of polymorphisms in the apolipoprotein APOA1-C3-A5 gene cluster with acute coronary syndrome. J Biomed Biotechnol. 2012;2012:509420.

2. Gotto AM Jr. Triglyceride as a risk factor for coronary artery disease. Am J Cardiol. 1998;82(9A):22Q–5Q.

3. Rade N, Pejic M, Daniel M, Lee T. Hypertriglyceridemia. J Am Board Fam Med. 2006;19:310–6.

4. Kao JT, et al. A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia. Hum Mol Genet. 2003;12(19):2533–9.

5. Charlton-Menys V, Durrington PN. Apolipoprotein A5 and hypertriglyceridemia. Clin Chem. 2005;51(2):295–7.

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