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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.344-345, 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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1 , 344-345.
YÜCESAN, E., Goncu, B. S., Aslanger, A., Ozgul, C., Hasanoglu, S., & Yesil, 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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 344-345.
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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, 344-345, 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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.344-345, 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 JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.344-345.
@article{article, 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}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={344-345} }