Yildiz, D. Et Al. 2022. Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation. KLINISCHE PADIATRIE , vol.234, no.04 , 244-245.

Yildiz, D., Yazici, M., Oguz, M. M., Torun, E. G., Sezer, A., & Kilic, M., (2022). Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation. KLINISCHE PADIATRIE , vol.234, no.04, 244-245.

Yildiz, Damla Et Al. "Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation," KLINISCHE PADIATRIE , vol.234, no.04, 244-245, 2022

Yildiz, Damla Et Al. "Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation." KLINISCHE PADIATRIE , vol.234, no.04, pp.244-245, 2022

Yildiz, D. Et Al. (2022) . "Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation." KLINISCHE PADIATRIE , vol.234, no.04, pp.244-245.

@article{article, author={Damla Yildiz Et Al. }, title={Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation}, journal={KLINISCHE PADIATRIE}, year=2022, pages={244-245} }