Altiokka-Uzun, G. Et Al. 2018. Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia. EPILEPTIC DISORDERS , vol.20, no.5 , 396-400.

Altiokka-Uzun, G., ÖZDEMİR, Ö., Ugur-Iseri, S., BEBEK, N., Gurses, C., ÖZBEK, U., ... BAYKAL, B.(2018). Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia. EPILEPTIC DISORDERS , vol.20, no.5, 396-400.

Altiokka-Uzun, Gunes Et Al. "Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia," EPILEPTIC DISORDERS , vol.20, no.5, 396-400, 2018

Altiokka-Uzun, Gunes Et Al. "Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia." EPILEPTIC DISORDERS , vol.20, no.5, pp.396-400, 2018

Altiokka-Uzun, G. Et Al. (2018) . "Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia." EPILEPTIC DISORDERS , vol.20, no.5, pp.396-400.

@article{article, author={Gunes Altiokka-Uzun Et Al. }, title={Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia}, journal={EPILEPTIC DISORDERS}, year=2018, pages={396-400} }