Hereditary hemochromatosis gene mutations in patients with myocardial infarction
Hereditary hemochromatosis (HH) is a disorder of iron accumulation in tissues, which is related to coronary heart diseases. Free radicals and reactive oxygen species, created because of iron deposition, promote oxidation of LDL cholesterol and could lead to the development of atherosclerosis. Studie...
| Permalink: | http://skupni.nsk.hr/Record/nsk.NSK01001079630/Similar |
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| Matična publikacija: |
Molecular and experimental biology in medicine 2 (2019), 1 ; str. 24-28 |
| Glavni autori: | Škrlec, Ivana (Author), Steiner, Robert, liječnik, Wagner, Jasenka |
| Vrsta građe: | e-članak |
| Jezik: | eng |
| Predmet: | |
| Online pristup: |
https://doi.org/10.33602/mebm.2.1.4 Molecular and experimental biology in medicine Hrčak |
APA stil citiranja
Škrlec, I. (2019). Hereditary hemochromatosis gene mutations in patients with myocardial infarction: Hereditary hemochromatosis gene mutations in patients with myocardial infarction [Elektronička građa]. Molecular and experimental biology in medicine.
Chicago stil citiranjaŠkrlec, Ivana. "Hereditary hemochromatosis gene mutations in patients with myocardial infarction: Hereditary hemochromatosis gene mutations in patients with myocardial infarction [Elektronička građa]." 2019.
MLA stil citiranjaŠkrlec, Ivana. "Hereditary hemochromatosis gene mutations in patients with myocardial infarction: Hereditary hemochromatosis gene mutations in patients with myocardial infarction [Elektronička građa]." 2019.