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dc.contributor.authorDizdarer, Gulsen
dc.contributor.authorAyta, Semih
dc.contributor.authorTutkavul, Kemal
dc.contributor.authorComu, Sinan
dc.contributor.authorMeral, Cihan
dc.contributor.authorAgan, Kadriye
dc.contributor.authorCaglayan, Server Hande
dc.contributor.authorTatli, Burak
dc.contributor.authorOzkara, Cigdem
dc.contributor.authorBaykan, BETÜL
dc.contributor.authorYapici, Zühal
dc.contributor.authorBebek, Nerses
dc.contributor.authorYalcin, Ozlem
dc.contributor.authorYalcin, Destina
dc.contributor.authorTÜRKDOĞAN, DİLŞAD
dc.contributor.authorUnalp, Aycan
dc.contributor.authorUluduz, Derya
dc.contributor.authorGul, Gunay
dc.contributor.authorKuscu, Demet
dc.date.accessioned2021-03-06T11:55:06Z
dc.date.available2021-03-06T11:55:06Z
dc.date.issued2011
dc.identifier.citationYalcin O., Baykan B., Agan K., Yapici Z., Yalcin D., Dizdarer G., TÜRKDOĞAN D., Ozkara C., Unalp A., Uluduz D., et al., "An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures", EPILEPSIA, cilt.52, ss.975-983, 2011
dc.identifier.issn0013-9580
dc.identifier.othervv_1032021
dc.identifier.otherav_f16180d4-35a2-4c8a-9d17-2faa5ab3b673
dc.identifier.urihttp://hdl.handle.net/20.500.12627/158355
dc.identifier.urihttps://doi.org/10.1111/j.1528-1167.2010.02970.x
dc.description.abstractPurpose: To further evaluate the previously shown linkage of absence epilepsy (AE) to 2q36, both in human and WAG/Rij absence rat models, a 160-kb region at 2q36 containing eight genes with expressions in the brain was targeted in a case-control association study involving 205 Turkish patients with AE and 219 controls.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.titleAn association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures
dc.typeMakale
dc.relation.journalEPILEPSIA
dc.contributor.departmentIstanbul Sisli Hamidiye Etfal Training & Research Hospital , ,
dc.identifier.volume52
dc.identifier.issue5
dc.identifier.startpage975
dc.identifier.endpage983
dc.contributor.firstauthorID60807


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