YILDIRIM, 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.

YILDIRIM, 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.

YILDIRIM, SEMA 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

YILDIRIM, SEMA 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

YILDIRIM, 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={SEMA YILDIRIM 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} }