YILDIRIM, M. Et Al. 2022. A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene. MOLECULAR SYNDROMOLOGY , vol.13, no.2 , 139-145.

YILDIRIM, M., BEKTAŞ, Ö., Tuncez, E., YENİAY SÜT, N., Sayar, Y., Oncul, U., ... TEBER, S.(2022). A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene. MOLECULAR SYNDROMOLOGY , vol.13, no.2, 139-145.

YILDIRIM, MİRAÇ Et Al. "A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene," MOLECULAR SYNDROMOLOGY , vol.13, no.2, 139-145, 2022

YILDIRIM, MİRAÇ Et Al. "A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene." MOLECULAR SYNDROMOLOGY , vol.13, no.2, pp.139-145, 2022

YILDIRIM, M. Et Al. (2022) . "A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene." MOLECULAR SYNDROMOLOGY , vol.13, no.2, pp.139-145.

@article{article, author={MİRAÇ YILDIRIM Et Al. }, title={A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene}, journal={MOLECULAR SYNDROMOLOGY}, year=2022, pages={139-145} }