Basit öğe kaydını göster

dc.contributor.authorDomingo, Cecile
dc.contributor.authorTouitou, Isabelle
dc.contributor.authorBayou, Anne
dc.contributor.authorOzen, Seza
dc.contributor.authorNotarnicola, Cecile
dc.contributor.authorDewalle, Marie
dc.contributor.authorDemaille, Jacques
dc.contributor.authorBuades, Rene
dc.contributor.authorSayadat, Chalom
dc.contributor.authorLevy, Micha
dc.contributor.authorBen-Chetrit, Eldad
dc.date.accessioned2019-12-10T10:37:18Z
dc.date.available2019-12-10T10:37:18Z
dc.date.issued2000
dc.identifier.issn1018-4813
dc.identifier.urihttps://doi.org/10.1038/sj.ejhg.5200462
dc.identifier.urihttp://hdl.handle.net/11655/13999
dc.description.abstractFamilial Mediterranean fever (FMF) is a hereditary disease commonly found among Jews, Armenians, Turks and Arabs. Recently, FMF was found in the 'Chuetas', a unique community on the island of Mallorca (Spain). To address the question of their possible Jewish origin, we analysed markers known to be linked to the gene responsible for FMF in Jews (MEFV) in this population. We found that 1/3 of the 16p13.3 chromosomes of the 'Chuetas' FMF patients bore the major ancestral haplotypes (S,S2) and their corresponding M694V and E148Q mutations, displayed by Jews from North Africa. Furthermore, we also detected a novel mutation (L110P) in this community. Yet 2/3 of these patients bore S negative haplotypes and lack the mutations commonly known to cause FMF. These results confirm that at least some of the 'Chuetas' share a common origin with Jews. However, they also provide evidence for the possibility of genetic heterogeneity in this disorder.
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.isversionof10.1038/sj.ejhg.5200462
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectBiochemistry & Molecular Biology
dc.subjectGenetics & Heredity
dc.titleFamilial Mediterranean Fever In The 'Chuetas' Of Mallorca: A Question Of Jewish Origin Or Genetic Heterogeneity
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalEuropean Journal Of Human Genetics
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume8
dc.identifier.issue4
dc.identifier.startpage242
dc.identifier.endpage246
dc.description.indexWoS
dc.description.indexScopus


Bu öğenin dosyaları:

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster