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• W1804940407 abstract "Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by attacks of fever and serosal inflammation; the biochemical basis is unknown. We recently reported linkage of the gene causing FMF (designated MEF) to two markers on chromosome 16p. To map MEF more precisely, we have now tested nine 16p markers. Two-point and multipoint linkage analysis, as well as a study of recombinant haplotypes, placed MEF between D16S94 and D16S80, a genetic interval of about 9 cM. We also examined rates of homozygosity for markers in this region, among offspring of consanguineous marriages. For eight of nine markers, the rate of homozygosity among 26 affected inbred individuals was higher than that among their 20 unaffected sibs. Localizing MEF more precisely on the basis of homozygosity rates alone would be difficult, for two reasons: First, the high FMF carrier frequency increases the chance that inbred offspring could have the disease without being homozygous by descent at MEF. Second, several of the markers in this region are relatively nonpolymorphic, with a high rate of homozygosity, regardless of their chromosomal location." @default.
• W1804940407 created "2016-06-24" @default.
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• W1804940407 date "1993-08-01" @default.
• W1804940407 modified "2023-09-27" @default.
• W1804940407 title "Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies." @default.
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• W1804940407 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1682355" @default.
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