Olgac, A. Et Al. 2020. A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation. Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1 , 165-170.

Olgac, A., Öztoprak, Ü., Kasapkara, Ç. S., Klllç, M., Yüksel, D., Derinkuyu, E. B., ... Taşçl Ylldlz, Y.(2020). A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation. Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, 165-170.

Olgac, Asburce Et Al. "A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation," Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, 165-170, 2020

Olgac, Asburce Et Al. "A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation." Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, pp.165-170, 2020

Olgac, A. Et Al. (2020) . "A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation." Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, pp.165-170.

@article{article, author={Asburce Olgac Et Al. }, title={A rare case of primary coenzyme Q10 deficiency due to COQ9 mutation}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2020, pages={165-170} }