Yigit, G. Et Al. 2022. Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.. Journal of medical genetics , vol.59, no.6 , 549-553.

Yigit, G., Sheffer, R., Daana, M., Li, Y., Kaygusuz, E., Mor-Shakad, H., ... Altmüller, J.(2022). Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.. Journal of medical genetics , vol.59, no.6, 549-553.

Yigit, Gökhan Et Al. "Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.," Journal of medical genetics , vol.59, no.6, 549-553, 2022

Yigit, Gökhan Et Al. "Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.." Journal of medical genetics , vol.59, no.6, pp.549-553, 2022

Yigit, G. Et Al. (2022) . "Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.." Journal of medical genetics , vol.59, no.6, pp.549-553.

@article{article, author={Gökhan Yigit Et Al. }, title={Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state.}, journal={Journal of medical genetics}, year=2022, pages={549-553} }