Demirbaş, H. Et Al. 2019. A rare etiology of epileptic encephalopathy: HECW2 mutations. European Journal Of Human Genetics , vol.27 , 1435.

Demirbaş, H., Özbudak, P., Serdaroğlu, A., Ergün, M. A., & Perçin, F. E., (2019). A rare etiology of epileptic encephalopathy: HECW2 mutations. European Journal Of Human Genetics , vol.27, 1435.

Demirbaş, Hakan Et Al. "A rare etiology of epileptic encephalopathy: HECW2 mutations," European Journal Of Human Genetics , vol.27, 1435, 2019

Demirbaş, Hakan Et Al. "A rare etiology of epileptic encephalopathy: HECW2 mutations." European Journal Of Human Genetics , vol.27, pp.1435, 2019

Demirbaş, H. Et Al. (2019) . "A rare etiology of epileptic encephalopathy: HECW2 mutations." European Journal Of Human Genetics , vol.27, p.1435.

@article{article, author={Hakan Demirbaş Et Al. }, title={A rare etiology of epileptic encephalopathy: HECW2 mutations}, journal={European Journal Of Human Genetics}, year=2019, pages={1435} }