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- W2024906008 abstract "FMF is considered an autosomal recessive autoinflammatory syndrome caused by single gene (MEFV) mutations. Recently, it has been known that also heterozygous mutation carriers can suffer from a mild or incomplete form of FMF, named FMF-like disease. Among Armenians, who have relatively high carrier rate of MEFV mutations, single mutation has been detected in about 1/5 of symptomatic cases. Thus, one cannot exclude the influence of other modifier genes and/or environmental factors which can contribute to the variable penetrance and to the phenotypic variability of FMF-like disease." @default.
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- W2024906008 date "2013-11-01" @default.
- W2024906008 modified "2023-10-16" @default.
- W2024906008 title "PW01-032 – FMF-like state: genetic factors unrelated to MEFV" @default.
- W2024906008 doi "https://doi.org/10.1186/1546-0096-11-s1-a85" @default.
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