M. Ozmen Et Al. , "Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients," ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3, pp.178-181, 2011
Ozmen, M. Et Al. 2011. Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3 , 178-181.
Ozmen, M., Dilber, C., Tatli, B., Aydinli, N., Caliskan, M., & Ekici, B., (2011). Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3, 178-181.
Ozmen, Meral Et Al. "Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients," ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3, 178-181, 2011
Ozmen, Meral Et Al. "Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3, pp.178-181, 2011
Ozmen, M. Et Al. (2011) . "Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.14, no.3, pp.178-181.
@article{article, author={Meral Ozmen Et Al. }, title={Severe myoclonic epilepsy of infancy (Dravet syndrome): Clinical and genetic features of nine Turkish patients}, journal={ANNALS OF INDIAN ACADEMY OF NEUROLOGY}, year=2011, pages={178-181} }