E. YÜCESAN Et Al. , "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," European Human Genetics Conference , 2020
YÜCESAN, E. Et Al. 2020. 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. European Human Genetics Conference .
YÜCESAN, E., Göncü, B., ASLANGER, A. D., Hasanoğlu, S., & YEŞİL SAYIN, G., (2020). 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 . European Human Genetics Conference
YÜCESAN, EMRAH Et Al. "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," European Human Genetics Conference, 2020
YÜCESAN, EMRAH Et Al. "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." European Human Genetics Conference , 2020
YÜCESAN, E. Et Al. (2020) . "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." European Human Genetics Conference .
@conferencepaper{conferencepaper, author={EMRAH YÜCESAN Et Al. }, title={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}, congress name={European Human Genetics Conference}, city={}, country={}, year={2020}}