Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Presentation of a new mutation in FMF and evaluating the frequency of distribution of the MEFV gene mutation in our region with clinical findings.

Molecular biology reports - 1 Mar 2021

Arpacı Abdullah, Doğan Serdar, Erdoğan Hazal Fatma, El Çiğdem, Cura Sibel Elmacıoğlu

Abstract excerpt

Familial Mediterranean Fever (FMF), which is an autosomal recessive disease characterized by recurrent self-limiting fever, peritonitis, pleuritis, arthritis and erysipelas-like erythemas, has been common among ethnic groups such as Turkish, Armenian, Arabic and Jewish. The clinical presentation is caused by mutations in the MEFV gene encoding the Pyrin protein. In this study, we aimed to present a new mutation...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged, 80 and over
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Familial Mediterranean Fever

Share to Infant

Share to Infant, Newborn

Share to Mutation Rate

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 33738724
DOI: 10.1007/s11033-020-06040-y
PMCID: PMC8060170

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Presentation of a new mutation in FMF and evaluating the frequency of distribution of the MEFV gene mutation in our region with clinical findings.PMID 33738724Read ↗

The spectrum of FMF mutations and genotypes in the referrals to molecular genetic laboratory at Kirikkale University in Turkey.Semantic proximity Read ↗

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia.Semantic proximity Read ↗

Screening of common and novel familial mediterranean fever mutations in south-east part of Turkey.Semantic proximity Read ↗

The spectrum of Familial Mediterranean Fever gene (MEFV) mutations and genotypes in Iran, and report of a novel missense variant (R204H).Semantic proximity Read ↗

R202Q prevalence in clinically diagnosed Familial Mediterranean Fever patients: 9 years of data analysis from 1570 patients living Central Black Sea region, Turkey.Semantic proximity Read ↗

Analysis of familial Mediterranean fever gene mutations in 202 patients with familial Mediterranean fever.Semantic proximity Read ↗

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.Semantic proximity Read ↗

Is Turkish MEFV Mutations Spectrum Different Among Regions?Semantic proximity Read ↗

Familial Mediterranean fever gene mutation frequencies and genotype-phenotype correlations in the Aegean region of Turkey.Semantic proximity Read ↗

Molecular analyses of MEFV gene mutation variants in Turkish population.Semantic proximity Read ↗

[Clinical and genetic analysis of a family with autosomal dominant-familial Mediterranean fever].Semantic proximity Read ↗

Updates on the molecular spectrum of MEFV variants in lebanese patients with Familial Mediterranean FeverSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.