Frequency of the R202Q mutation of MEFV gene in Iranian patients with premature coronary artery disease: a report from West Azerbaijan province of Iran-Reference-Cited by-同舟云学术

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Frequency of the R202Q mutation of MEFV gene in Iranian patients with premature coronary artery disease: a report from West Azerbaijan province of Iran

Published:2024-04-01 Issue:2 Volume:3 Page:84-89
ISSN:0535-6180
Container-title:Health Science Monitor
language:en
Short-container-title:Health Science Monitor

Author:

Bagheri Morteza,Khadem-Vatani Kamal,Abdi Rad Isa^ORCID,Seyed-Mohammadzad MirHossein,Rostamzadeh Alireza,Rahimi Behzad,Kavosi Negin

Publisher

Apex Publishing

Link

https://hsm.umsu.ac.ir/article-1-137-en.pdf

Reference20 articles.

1. Risk factors for premature coronary artery disease (PCAD) in adults: a systematic review protocol

2. Rasmi Y, Bagheri M, Faramarz-Gaznagh S, Nemati M, Khadem-Ansari MH, Saboory E, et al. Transcriptional activity of tumor necrosis factor-alpha gene in peripheral blood mononuclear cells in patients with coronary slow flow. ARYA Atherosclerosis 2017; 13(4):196-201.

3. Tumor Necrosis Factor-alpha Gene Expression in PBMCs of Iranian Azeri Turkish Patients with Premature Coronary Artery Disease (Age ≤50 Years)

4. Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran

5. TNF receptor type 1 and TNF receptor type 2 mRNA expression was not associated with coronary artery disease in a group of Iranian Turks

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