Yazar "Yücesan, Emrah" için Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed listeleme
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Identification and functional characterization of a novel homozygous mutation in KCNMA1 encoding voltage and calcium sensitive potassium channel is associated with dyskinesia, epilepsy, intellectual disability, cerebellar and corticospinal tract atrophy
Yücesan, Emrah; Goncu, Beyza; Aslanger, Ayça Dilruba; Özgül, Cemil; Hasanoğlu, Sevde; Yeşil, Gözde (Springer Nature, 2020)... -
Two rare autosomal recessive neurological disorders identified by combined genetic approaches in a single consanguineous family with multiple offspring
Süsgün, Seda; Yücesan, Emrah; Göncü, Beyza; Hasanoğlu Sayın, Sevde; Kına, Ümit Yaşar; Özgül, Cemil; Düzenli, Ömer Faruk; Kocatürk, Özcan; Çalık, Mustafa; Özbek, Uğur; Uğur İşeri, Sibel Aylin (2024)Introduction: Neurodevelopmental disorders (NDDs) refer to a broad range of diseases including developmental delay, intellectual disability, epilepsy, autism spectrum disorders, and attention-deficit/hyperactivity disorder ...