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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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| Publicat a: | Mediterr J Rheumatol |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Mediterranean Journal of Rheumatology (MJR)
2020
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| Matèries: | |
| Accés en línia: | 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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