E. YÜCESAN Et Al. , "Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy," INTERNATIONAL JOURNAL OF NEUROSCIENCE , 2023
YÜCESAN, E. Et Al. 2023. Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy. INTERNATIONAL JOURNAL OF NEUROSCIENCE .
YÜCESAN, E., GÖNCÜ, B. S., ÖZGÜL, C., Kebapci, A., Aslanger, A. D., Akyuz, E., ... YEŞİL SAYIN, G.(2023). Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy. INTERNATIONAL JOURNAL OF NEUROSCIENCE .
YÜCESAN, EMRAH Et Al. "Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy," INTERNATIONAL JOURNAL OF NEUROSCIENCE , 2023
YÜCESAN, EMRAH Et Al. "Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy." INTERNATIONAL JOURNAL OF NEUROSCIENCE , 2023
YÜCESAN, E. Et Al. (2023) . "Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy." INTERNATIONAL JOURNAL OF NEUROSCIENCE .
@article{article, author={EMRAH YÜCESAN Et Al. }, title={Functional characterization of KCNMA1 mutation associated with dyskinesia, seizure, developmental delay, and cerebellar atrophy}, journal={INTERNATIONAL JOURNAL OF NEUROSCIENCE}, year=2023}