Clinical Evaluation of a Reverse Hybridization Assay for the Molecular Detection of Twelve MEFV Gene Mutations
Author:
Affiliation:
1. Service de Biochimie et de Génétique Moléculaire, Hôpital Henri Mondor, AP-HP, 94010 Créteil, France
2. INSERM U468 Génétique Moléculaire et Physiopathologie, 94010 Créteil, France
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/49/11/1942/32736835/clinchem1942.pdf
Reference12 articles.
1. A candidate gene for familial Mediterranean fever
2. Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever
3. 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
4. Interaction between Pyrin and the Apoptotic Speck Protein (ASC) Modulates ASC-induced Apoptosis
5. Targeted Disruption of Pyrin, the FMF Protein, Causes Heightened Sensitivity to Endotoxin and a Defect in Macrophage Apoptosis
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3. Genotype – phenotype correlation in pediatric patients with Familial Mediterrenean Fever;Journal of Dr Behcet Uz Children s Hospital;2018
4. Subclinical Familial Mediterranean Fever and MEFV gene polymorphisms in Henoch–Schӧnlein purpura children: Relation to the clinical and laboratory characteristics of the disease;The Egyptian Rheumatologist;2016-10
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