Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation
Kesim, Yesim F, Uzun, Gunes Altiokka, Yucesan, Emrah, Tuncer, Feyza N, Ozdemir, Ozkan, Bebek, Nerses, Ozbek, Ugur, Iseri, Sibel A. Ugur, Baykan, Betul
Published in Epilepsy research (01.02.2016)
Published in Epilepsy research (01.02.2016)
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Journal Article
A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family
Tuncer, Feyza N, Gormez, Zeliha, Calik, Mustafa, Altiokka Uzun, Gunes, Sagiroglu, Mahmut S, Yuceturk, Betul, Yuksel, Bayram, Baykan, Betul, Bebek, Nerses, Iscan, Akin, Ugur Iseri, Sibel A, Ozbek, Ugur
Published in Epilepsy research (01.07.2015)
Published in Epilepsy research (01.07.2015)
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