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Genotype Mutations in Egyptian Children with Familial Mediterranean Fever: Clinical Profile, and Response to Colchicine

BACKGROUND: Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disorder that is characterized by recurrent episodes of fever, peritonitis, pleuritis, pericarditis, and/or arthritis. MEFV is the responsible gene for FMF, of which more than 310 mutations have been reported;...

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Detalhes bibliográficos
Publicado no:Mediterr J Rheumatol
Main Authors: Talaat, Hala S., Sheba, Maha F., Mohammed, Rehab H., Gomaa, Mohamed Ali, Rifaei, Nihal El, Ibrahim, Mohamed Farouk M.
Formato: Artigo
Idioma:Inglês
Publicado em: The Mediterranean Journal of Rheumatology (MJR) 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7362121/
https://ncbi.nlm.nih.gov/pubmed/32676558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.31138/mjr.31.2.206
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