Inan, B. Et Al. 2023. A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.. Acta neurologica Belgica , vol.123, no.5 , 1985-1987.

Inan, B., Azman, F., Aktas, D., Yildiz, Y., & Saygi, S., (2023). A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.. Acta neurologica Belgica , vol.123, no.5, 1985-1987.

Inan, Berin Et Al. "A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.," Acta neurologica Belgica , vol.123, no.5, 1985-1987, 2023

Inan, Berin Et Al. "A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.." Acta neurologica Belgica , vol.123, no.5, pp.1985-1987, 2023

Inan, B. Et Al. (2023) . "A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.." Acta neurologica Belgica , vol.123, no.5, pp.1985-1987.

@article{article, author={Berin Inan Et Al. }, title={A novel mutation in ATP13A2 gene in a patient with complicated hereditary spastic paraplegia accompanied by tubulopathy.}, journal={Acta neurologica Belgica}, year=2023, pages={1985-1987} }