![MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications - ScienceDirect MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0002929707637318-gr2.gif)
MEFV-Gene Analysis in Armenian Patients with Familial Mediterranean Fever: Diagnostic Value and Unfavorable Renal Prognosis of the M694V Homozygous Genotype—Genetic and Therapeutic Implications - ScienceDirect
![Life | Free Full-Text | Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene Life | Free Full-Text | Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene](https://www.mdpi.com/life/life-12-00631/article_deploy/html/images/life-12-00631-g001.png)
Life | Free Full-Text | Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene
![Spectrum of MEFV gene mutations in 4,256 familial Mediterranean fever patients from Iran: a comprehensive systematic review | Egyptian Journal of Medical Human Genetics | Full Text Spectrum of MEFV gene mutations in 4,256 familial Mediterranean fever patients from Iran: a comprehensive systematic review | Egyptian Journal of Medical Human Genetics | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs43042-022-00222-y/MediaObjects/43042_2022_222_Fig1_HTML.png)
Spectrum of MEFV gene mutations in 4,256 familial Mediterranean fever patients from Iran: a comprehensive systematic review | Egyptian Journal of Medical Human Genetics | Full Text
![Lack of clear and univocal genotype‐phenotype correlation in familial Mediterranean fever patients: A systematic review - Gangemi - 2018 - Clinical Genetics - Wiley Online Library Lack of clear and univocal genotype‐phenotype correlation in familial Mediterranean fever patients: A systematic review - Gangemi - 2018 - Clinical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4d568699-fe1f-4a04-bd67-f8f9a8e451e4/cge13223-fig-0001-m.jpg)
Lack of clear and univocal genotype‐phenotype correlation in familial Mediterranean fever patients: A systematic review - Gangemi - 2018 - Clinical Genetics - Wiley Online Library
![The regulation of MEFV expression and its role in health and familial Mediterranean fever | Genes & Immunity The regulation of MEFV expression and its role in health and familial Mediterranean fever | Genes & Immunity](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fgene.2011.53/MediaObjects/41435_2011_Article_BFgene201153_Fig1_HTML.jpg)
The regulation of MEFV expression and its role in health and familial Mediterranean fever | Genes & Immunity
Article: Familial Mediterranean Fever (FMF): a single centre retrospective study in Amsterdam (full text) - June 2019 - NJM
![Familial Mediterranean fever, Inflammation and Nephrotic Syndrome: Fibrillary Glomerulopathy and the M680I Missense Mutation | BMC Nephrology | Full Text Familial Mediterranean fever, Inflammation and Nephrotic Syndrome: Fibrillary Glomerulopathy and the M680I Missense Mutation | BMC Nephrology | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2F1471-2369-4-6/MediaObjects/12882_2003_Article_19_Fig3_HTML.jpg)
Familial Mediterranean fever, Inflammation and Nephrotic Syndrome: Fibrillary Glomerulopathy and the M680I Missense Mutation | BMC Nephrology | Full Text
![MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease | Annals of the Rheumatic Diseases MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease | Annals of the Rheumatic Diseases](https://ard.bmj.com/content/annrheumdis/73/2/455/F1.large.jpg)
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease | Annals of the Rheumatic Diseases
![JCM | Free Full-Text | The Frequency of MEFV Gene Mutations and Genotypes in Sanliurfa Province, South-Eastern Region of Turkey, after the Syrian Civil War by Using Next Generation Sequencing and Report JCM | Free Full-Text | The Frequency of MEFV Gene Mutations and Genotypes in Sanliurfa Province, South-Eastern Region of Turkey, after the Syrian Civil War by Using Next Generation Sequencing and Report](https://www.mdpi.com/jcm/jcm-07-00105/article_deploy/html/images/jcm-07-00105-g001.png)
JCM | Free Full-Text | The Frequency of MEFV Gene Mutations and Genotypes in Sanliurfa Province, South-Eastern Region of Turkey, after the Syrian Civil War by Using Next Generation Sequencing and Report
![Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia | Annals of Saudi Medicine Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia | Annals of Saudi Medicine](https://www.annsaudimed.net/cms/asset/4c0f885b-cc8e-4fd0-9e5e-30b15d730d08/asm-6-382.jpg)