Şeker-Yılmaz, B. Et Al. 2018. A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency.. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism. , (ATİNA, Greece).

Şeker-Yılmaz, B., KOR, D., BULUT, F. D., KILAVUZ, S., & ÖNENLİ MUNGAN, H. N., (2018). A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency. . Annual Symposium of the Society for the Study of Inborn Errors of Metabolism., ATİNA, Greece

Şeker-Yılmaz, Berna Et Al. "A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency.," Annual Symposium of the Society for the Study of Inborn Errors of Metabolism., ATİNA, Greece, 2018

Şeker-Yılmaz, Berna Et Al. "A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency.." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism. , ATİNA, Greece, 2018

Şeker-Yılmaz, B. Et Al. (2018) . "A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency.." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism. , ATİNA, Greece.

@conferencepaper{conferencepaper, author={Berna Şeker-Yılmaz Et Al. }, title={A novel FASTKD2 gene mutation presenting with mitochondrial cytochrome c oxidase deficiency.}, congress name={Annual Symposium of the Society for the Study of Inborn Errors of Metabolism.}, city={ATİNA}, country={Greece}, year={2018}}