Sager, G. Et Al. 2023. Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.44 , 51-56.

Sager, G., TÜRKYILMAZ, A., Gunbey, H. P., Tas, I., Ozhelvaci, F., & Akin, Y., (2023). Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.44, 51-56.

Sager, Gunes Et Al. "Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood," EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.44, 51-56, 2023

Sager, Gunes Et Al. "Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.44, pp.51-56, 2023

Sager, G. Et Al. (2023) . "Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood." EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.44, pp.51-56.

@article{article, author={Gunes Sager Et Al. }, title={Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood}, journal={EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY}, year=2023, pages={51-56} }