Özsoy, Ö. Et Al. 2023. A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature. NEUROLOGY ASIA , vol.28 , 421-429.

Özsoy, Ö., Cinleti, T., Zeybek, S., Soydemir, D., Sarıkaya Uzan, G., Günay, Ç., ... Hız, A. S.(2023). A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature. NEUROLOGY ASIA , vol.28, 421-429.

Özsoy, ÖZLEM Et Al. "A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature," NEUROLOGY ASIA , vol.28, 421-429, 2023

Özsoy, ÖZLEM Et Al. "A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature." NEUROLOGY ASIA , vol.28, pp.421-429, 2023

Özsoy, Ö. Et Al. (2023) . "A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature." NEUROLOGY ASIA , vol.28, pp.421-429.

@article{article, author={ÖZLEM ÖZSOY Et Al. }, title={A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature}, journal={NEUROLOGY ASIA}, year=2023, pages={421-429} }