Gursoy, S. Et Al. 2020. Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2 , 206-210.

Gursoy, S., Ataman, E., Baysal, B. T., Ozyilmaz, B., Gencpinar, P., HIZ, A. S., ... YİŞ, U.(2020). Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy. ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2, 206-210.

Gursoy, SEMRA Et Al. "Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy," ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2, 206-210, 2020

Gursoy, SEMRA Et Al. "Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2, pp.206-210, 2020

Gursoy, S. Et Al. (2020) . "Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy." ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2, pp.206-210.

@article{article, author={SEMRA GÜRSOY Et Al. }, title={Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy}, journal={ANNALS OF INDIAN ACADEMY OF NEUROLOGY}, year=2020, pages={206-210} }