Genç Sel, Ç. Et Al. 2020. A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome. Neurology Asia , vol.25, no.3 , 403-413.

Genç Sel, Ç., CEYLAN, A. C., Yayici Köken, Ö., Yüksel, D., & Oğuz, K. K., (2020). A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome. Neurology Asia , vol.25, no.3, 403-413.

Genç Sel, Çiğdem Et Al. "A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome," Neurology Asia , vol.25, no.3, 403-413, 2020

Genç Sel, Çiğdem G. Et Al. "A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome." Neurology Asia , vol.25, no.3, pp.403-413, 2020

Genç Sel, Ç. Et Al. (2020) . "A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome." Neurology Asia , vol.25, no.3, pp.403-413.

@article{article, author={Çiğdem Genç Sel Et Al. }, title={A rare neurodegenerative disorder with a novel mutation in rogdi and rett-like phenotype: Kohlschütter-tönz syndrome}, journal={Neurology Asia}, year=2020, pages={403-413} }