Köse, M. D. Et Al. 2020. Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13. Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1 , 157-163.

Köse, M. D., Kagnici, M., Özdemir, T. R., Erdur, C. B., Erdemir, G., Karakoyun, M., ... Guzin, Y.(2020). Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13. Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, 157-163.

Köse, Melis Et Al. "Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13," Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, 157-163, 2020

Köse, Melis D. Et Al. "Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13." Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, pp.157-163, 2020

Köse, M. D. Et Al. (2020) . "Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13." Journal of Pediatric Endocrinology and Metabolism , vol.33, no.1, pp.157-163.

@article{article, author={Melis Demir Köse Et Al. }, title={Clinical findings in five Turkish patients with citrin deficiency and identification of a novel mutation on SLC25A13}, journal={Journal of Pediatric Endocrinology and Metabolism}, year=2020, pages={157-163} }