Akar, H. T. Et Al. 2024. The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23). Zeitschrift fur Geburtshilfe und Neonatologie , vol.229, no.1 , 60-62.

Akar, H. T., Akduman, H., Kolkıran, A., Taşadelen, E., & Aycan, N., (2024). The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23). Zeitschrift fur Geburtshilfe und Neonatologie , vol.229, no.1, 60-62.

Akar, Halil Et Al. "The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23)," Zeitschrift fur Geburtshilfe und Neonatologie , vol.229, no.1, 60-62, 2024

Akar, Halil T. Et Al. "The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23)." Zeitschrift fur Geburtshilfe und Neonatologie , vol.229, no.1, pp.60-62, 2024

Akar, H. T. Et Al. (2024) . "The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23)." Zeitschrift fur Geburtshilfe und Neonatologie , vol.229, no.1, pp.60-62.

@article{article, author={Halil Tuna Akar Et Al. }, title={The rare reason for massive lactic aciduria and mitochondrial disorders: combined oxidative phosphorylation deficiency type 23 (COXPD23)}, journal={Zeitschrift fur Geburtshilfe und Neonatologie}, year=2024, pages={60-62} }