O. Gungor Et Al. , "A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.," Genetic counseling (Geneva, Switzerland) , vol.26, no.1, pp.41-6, 2015
Gungor, O. Et Al. 2015. A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.. Genetic counseling (Geneva, Switzerland) , vol.26, no.1 , 41-6.
Gungor, O., Ozkaya, A. K., Hirfanoglu, T., Dilber, C., & Aydin, K., (2015). A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.. Genetic counseling (Geneva, Switzerland) , vol.26, no.1, 41-6.
Gungor, O. Et Al. "A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.," Genetic counseling (Geneva, Switzerland) , vol.26, no.1, 41-6, 2015
Gungor, O. Et Al. "A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.." Genetic counseling (Geneva, Switzerland) , vol.26, no.1, pp.41-6, 2015
Gungor, O. Et Al. (2015) . "A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.." Genetic counseling (Geneva, Switzerland) , vol.26, no.1, pp.41-6.
@article{article, author={O. Gungor Et Al. }, title={A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report.}, journal={Genetic counseling (Geneva, Switzerland)}, year=2015, pages={41-6} }