Oner, T. O. Et Al. 2021. OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development. EPILEPTIC DISORDERS , vol.23, no.6 , 843-853.

Oner, T. O., Unalp, A., Hiz, S., Bayram, E., Kaytan, I., & Cingoz, S., (2021). OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development. EPILEPTIC DISORDERS , vol.23, no.6, 843-853.

Oner, Tulay Et Al. "OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development," EPILEPTIC DISORDERS , vol.23, no.6, 843-853, 2021

Oner, Tulay O. Et Al. "OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development." EPILEPTIC DISORDERS , vol.23, no.6, pp.843-853, 2021

Oner, T. O. Et Al. (2021) . "OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development." EPILEPTIC DISORDERS , vol.23, no.6, pp.843-853.

@article{article, author={Tulay Oncu Oner Et Al. }, title={OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development}, journal={EPILEPTIC DISORDERS}, year=2021, pages={843-853} }