G. TARHAN Et Al. , "Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis," 32nd European Neurology Congres and 12th International Conference on Vascular Dementia , Londrina, Brazil, 2019
TARHAN, G. Et Al. 2019. Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis. 32nd European Neurology Congres and 12th International Conference on Vascular Dementia , (Londrina, Brazil).
TARHAN, G., HIZ, Ş. F., İNANIR, B. E., BAŞAK, A. N., ŞİMŞİR, G., & NACAR DOĞAN, S., (2019). Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis . 32nd European Neurology Congres and 12th International Conference on Vascular Dementia, Londrina, Brazil
TARHAN, GÜLLÜ Et Al. "Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis," 32nd European Neurology Congres and 12th International Conference on Vascular Dementia, Londrina, Brazil, 2019
TARHAN, GÜLLÜ Et Al. "Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis." 32nd European Neurology Congres and 12th International Conference on Vascular Dementia , Londrina, Brazil, 2019
TARHAN, G. Et Al. (2019) . "Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis." 32nd European Neurology Congres and 12th International Conference on Vascular Dementia , Londrina, Brazil.
@conferencepaper{conferencepaper, author={GÜLLÜ TARHAN Et Al. }, title={Two homozygous KIF1C mutations in a Turkish family with cerebellar dysfunction and spastic paraparesis}, congress name={32nd European Neurology Congres and 12th International Conference on Vascular Dementia}, city={Londrina}, country={Brazil}, year={2019}}