Öztürk, S. Et Al. 2022. Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.. Pediatric neurology , vol.136 , 43-49.

Öztürk, S., Güleç, A., Erdoğan, M., Demir, M., Canpolat, M., Gümüş, H., ... Çağlayan, A. O.(2022). Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.. Pediatric neurology , vol.136, 43-49.

Öztürk, Selcan Et Al. "Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.," Pediatric neurology , vol.136, 43-49, 2022

Öztürk, Selcan Et Al. "Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.." Pediatric neurology , vol.136, pp.43-49, 2022

Öztürk, S. Et Al. (2022) . "Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.." Pediatric neurology , vol.136, pp.43-49.

@article{article, author={Selcan Öztürk Et Al. }, title={Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With Three Novel Mutations.}, journal={Pediatric neurology}, year=2022, pages={43-49} }