Demirbas, M. H. Et Al. 2019. A rare etiology of epileptic encephalopathy: HECW2 mutations. 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , (Gothenburg, Sweden), 1435.

Demirbas, M. H., Ozbudak, P., Serdaroglu, A., Ergun, M. A., & Percin, E. F., (2019). A rare etiology of epileptic encephalopathy: HECW2 mutations . 52nd Conference of the European-Society-of-Human-Genetics (ESHG) (pp.1435). Gothenburg, Sweden

Demirbas, M. Et Al. "A rare etiology of epileptic encephalopathy: HECW2 mutations," 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 2019

Demirbas, M. H. Et Al. "A rare etiology of epileptic encephalopathy: HECW2 mutations." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1435, 2019

Demirbas, M. H. Et Al. (2019) . "A rare etiology of epileptic encephalopathy: HECW2 mutations." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, p.1435.

@conferencepaper{conferencepaper, author={M. H. Demirbas Et Al. }, title={A rare etiology of epileptic encephalopathy: HECW2 mutations}, congress name={52nd Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1435} }