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}}