Funder
Hormozgan University of Medical Sciences
Subject
Genetics(clinical),Genetics
Reference29 articles.
1. Endothelial nitric oxide synthase gene-922A> G,-786 T> C, 4b/4a, and 894 G> T variants and premature coronary artery disease: an association study with haplotype analysis;Aghabozorgi;Meta Gene,2019
2. Genetic polymorphism of CYP2D6 gene among Egyptian hypertensive cases;Ali;J. Basic Appl. Zool.,2013
3. Impact of genotype-predicted CYP2D6 metabolism on clinical effects and tolerability of metoprolol in patients after myocardial infarction - a prospective observational study;Anstensrud;Eur. J. Clin. Pharmacol.,2020
4. CYP 2D6*4 polymorphism and interindividual response variation to metoprolol in stage 1 hypertensive patients: no association in a rural Indian population?;Ayyappadihas;Turk. J. Med. Sci.,2015
5. Prevalence of the CYP2D6*10 (C100T), *4 (G1846A), and *14 (G1758A) alleles among Iranians of different ethnicities;Bagheri;Drug Des. Devel. Ther.,2015
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献