Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation von Kesim, Yesim F, Uzun, Gunes Altiokka, Yucesan, Emrah, Tuncer, Feyza N, Ozdemir, Ozkan, Bebek, Nerses, Ozbek, Ugur, Iseri, Sibel A. Ugur, Baykan, Betul

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A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family von 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

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