Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
dc.contributor.author | Ozdemir, Ozturk | |
dc.contributor.author | Sezgin, Ilhan | |
dc.contributor.author | Kurtulgan, Hande Kucuk | |
dc.contributor.author | Candan, Ferhan | |
dc.contributor.author | Koksal, Binnur | |
dc.contributor.author | Sumer, Haldun | |
dc.contributor.author | Icagasioglu, Dilara | |
dc.contributor.author | Uslu, Atilla | |
dc.contributor.author | Yildiz, Fazilet | |
dc.contributor.author | Arslan, Sulhattin | |
dc.contributor.author | Cetinkaya, Selma | |
dc.contributor.author | Citli, Senol | |
dc.contributor.author | Oztemur, Zekeriya | |
dc.contributor.author | Kayatas, Mansur | |
dc.date.accessioned | 2019-07-27T12:10:23Z | |
dc.date.accessioned | 2019-07-28T10:05:36Z | |
dc.date.available | 2019-07-27T12:10:23Z | |
dc.date.available | 2019-07-28T10:05:36Z | |
dc.date.issued | 2011 | |
dc.identifier.issn | 0301-4851 | |
dc.identifier.uri | https://dx.doi.org/10.1007/s11033-010-9991-7 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12418/9542 | |
dc.description | WOS: 000290102100044 | en_US |
dc.description | PubMed ID: 20165923 | en_US |
dc.description.abstract | The Familial Mediterranean Fever (FMF) shows an autosomal recessive pattern of inheritance and affects certain ethnic groups. Disease is caused by mutations in MEFV gene and more than 180 mutations have been defined in affected individuals. Current study aimed to determine the frequency-type of the mutations for MEFV gene in Sivas-middle Anatolian city. The cohort was composed of 3340 patients. MEFV gene mutations were studied by multiplex PCR based reverse hybridization stripAssay method. Patients' clinical features were; family history: 68%, erysipelas-like erythema: 17.6%, fever: 89.9%, abdominal pain: 84.2%, peritonitis: 90.2%, arthritis: 33%, pleuritis: 14.2%, parental consanguinity: 21.2%. Current results revealed that M694V is the most frequent mutation (43.12%), followed by E148Q (20.18), M680I(G/C) (15.00%) and V726A (11.32%). The study population has a high rate of carriers and the E148Q mutation frequency was found to be highest when compared to the other regions of Turkey and other Mediterranean groups. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | SPRINGER | en_US |
dc.relation.isversionof | 10.1007/s11033-010-9991-7 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | FMF | en_US |
dc.subject | Allelic frequencies | en_US |
dc.subject | Sivas population | en_US |
dc.subject | Turkey | en_US |
dc.title | Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers | en_US |
dc.type | article | en_US |
dc.relation.journal | MOLECULAR BIOLOGY REPORTS | en_US |
dc.contributor.department | [Ozdemir, Ozturk -- Sezgin, Ilhan -- Kurtulgan, Hande Kucuk -- Koksal, Binnur -- Yildiz, Fazilet -- Citli, Senol] Cumhuriyet Univ, Dept Med Genet, Fac Med, TR-58140 Sivas, Turkey -- [Ozdemir, Ozturk] COMU Univ, Dept Med Genet, Fac Med, TR-17100 Canakkale, Turkey -- [Candan, Ferhan] Cumhuriyet Univ, Dept Interior Med, Fac Med, TR-58140 Sivas, Turkey -- [Sumer, Haldun -- Cetinkaya, Selma] Cumhuriyet Univ, Dept Publ Hlth, Fac Med, TR-58140 Sivas, Turkey -- [Icagasioglu, Dilara] Cumhuriyet Univ, Dept Pediat, Fac Med, TR-58140 Sivas, Turkey -- [Uslu, Atilla] Istanbul Univ, Dept Physiol, Fac Med, TR-34039 Istanbul, Turkey -- [Arslan, Sulhattin] Cumhuriyet Univ, Dept Thorax Dis, Fac Med, TR-58140 Sivas, Turkey -- [Oztemur, Zekeriya] Cumhuriyet Univ, Dept Ortopedia, Fac Med, TR-58140 Sivas, Turkey -- [Kayatas, Mansur] Cumhuriyet Univ, Dept Nephrol, Fac Med, TR-58140 Sivas, Turkey | en_US |
dc.contributor.authorID | Kurtulgan, Hande Kucuk -- 0000-0001-9172-3244; Oztemur, Zekeriya -- 0000-0003-2134-8797 | en_US |
dc.identifier.volume | 38 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.endpage | 3200 | en_US |
dc.identifier.startpage | 3195 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
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