Altıntaş, M. Et Al. 2023. A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy. 15th Congress of the European Paediatric Neurology Society (EPNS) , (Praha, Czech Republic), 580.

Altıntaş, M., Yıldırım, M., Yeniay Süt, N., Bektaş, Ö., & Teber, S., (2023). A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy . 15th Congress of the European Paediatric Neurology Society (EPNS) (pp.580). Praha, Czech Republic

Altıntaş, Mert Et Al. "A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy," 15th Congress of the European Paediatric Neurology Society (EPNS), Praha, Czech Republic, 2023

Altıntaş, Mert Et Al. "A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy." 15th Congress of the European Paediatric Neurology Society (EPNS) , Praha, Czech Republic, pp.580, 2023

Altıntaş, M. Et Al. (2023) . "A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy." 15th Congress of the European Paediatric Neurology Society (EPNS) , Praha, Czech Republic, p.580.

@conferencepaper{conferencepaper, author={Mert Altıntaş Et Al. }, title={A case of NDUFV1 gene mutation associated with mild developmental delay and cystic leukoencephalopathy}, congress name={15th Congress of the European Paediatric Neurology Society (EPNS)}, city={Praha}, country={Czech Republic}, year={2023}, pages={580} }