Yeniay Süt, N. Et Al. 2023. Episodic ataxia associated with SCN2A mutation: A case report. 15th Congress of the European Paediatric Neurology Society (EPNS) , (Praha, Czech Republic), 529.

Yeniay Süt, N., Yıldırım, M., Kartal, A. T., Bektaş, Ö., & Teber, S., (2023). Episodic ataxia associated with SCN2A mutation: A case report . 15th Congress of the European Paediatric Neurology Society (EPNS) (pp.529). Praha, Czech Republic

Yeniay Süt, Nurşah Et Al. "Episodic ataxia associated with SCN2A mutation: A case report," 15th Congress of the European Paediatric Neurology Society (EPNS), Praha, Czech Republic, 2023

Yeniay Süt, Nurşah Y. Et Al. "Episodic ataxia associated with SCN2A mutation: A case report." 15th Congress of the European Paediatric Neurology Society (EPNS) , Praha, Czech Republic, pp.529, 2023

Yeniay Süt, N. Et Al. (2023) . "Episodic ataxia associated with SCN2A mutation: A case report." 15th Congress of the European Paediatric Neurology Society (EPNS) , Praha, Czech Republic, p.529.

@conferencepaper{conferencepaper, author={Nurşah Yeniay Süt Et Al. }, title={Episodic ataxia associated with SCN2A mutation: A case report}, congress name={15th Congress of the European Paediatric Neurology Society (EPNS)}, city={Praha}, country={Czech Republic}, year={2023}, pages={529} }