MEFV gene mutation spectrum in patients with familial mediterranean fever
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference7 articles.
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2. Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype–genotype correlation;Mattit;Eur J Med Genet,2006
3. Genotype–phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis;Yalçınkaya;Rheumatology(Oxford),2000
4. Genotype-phenotype correlation in Japanese patients with familial Mediterranean fever: differences in genotype and clinical features between Japanese and Mediterranean populations;Kishida;Arthritis Res Ther,2014
5. Clinical and demographic evaluation according to MEFV genes in patients with familial mediterranean fever;Sönmezgöz;Biochem Genet,2019
Cited by 3 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
1. A narrative review on the role of cytokines in the pathogenesis and treatment of familial Mediterranean fever: an emphasis on pediatric cases;Frontiers in Pediatrics;2024-07-26
2. Molecular analyses of MEFV gene mutation variants in Turkish population;Molecular Biology Reports;2024-07-23
3. Unraveling the genome: Familial Mediterranean fever;Journal of the American Association of Nurse Practitioners;2024-01
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