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Yalcin, Ozlem; Baykan, Betul; Agan, Kadriye; Yapici, Zuhal; Yalcin, Destina; Dizdarer, Gulsen; Turkdogan, Dilsad; Ozkara, Cigdem; Unalp, Aycan; Uluduz, Derya; Gul, Gunay; Kuscu, Demet; Ayta, Semih; Tutkavul, Kemal; Comu, Sinan; Tatli, Burak; Meral, Cihan; Bebek, Nerses; Caglayan, Server Hande
<?xml version='1.0' encoding='utf-8'?> <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"> <dc:creator>Yalcin, Ozlem</dc:creator> <dc:creator>Baykan, Betul</dc:creator> <dc:creator>Agan, Kadriye</dc:creator> <dc:creator>Yapici, Zuhal</dc:creator> <dc:creator>Yalcin, Destina</dc:creator> <dc:creator>Dizdarer, Gulsen</dc:creator> <dc:creator>Turkdogan, Dilsad</dc:creator> <dc:creator>Ozkara, Cigdem</dc:creator> <dc:creator>Unalp, Aycan</dc:creator> <dc:creator>Uluduz, Derya</dc:creator> <dc:creator>Gul, Gunay</dc:creator> <dc:creator>Kuscu, Demet</dc:creator> <dc:creator>Ayta, Semih</dc:creator> <dc:creator>Tutkavul, Kemal</dc:creator> <dc:creator>Comu, Sinan</dc:creator> <dc:creator>Tatli, Burak</dc:creator> <dc:creator>Meral, Cihan</dc:creator> <dc:creator>Bebek, Nerses</dc:creator> <dc:creator>Caglayan, Server Hande</dc:creator> <dc:date>2011-01-01</dc:date> <dc:description>Purpose: 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:description> <dc:identifier>https://aperta.ulakbim.gov.trrecord/19201</dc:identifier> <dc:identifier>oai:zenodo.org:19201</dc:identifier> <dc:rights>info:eu-repo/semantics/openAccess</dc:rights> <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights> <dc:source>EPILEPSIA 52(5) 975-983</dc:source> <dc:title>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</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> <dc:type>publication-article</dc:type> </oai_dc:dc>
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