TAŞTEMEL ÖZTÜRK, T. Et Al. 2023. A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature. PEDIATRIC NEPHROLOGY , vol.38, no.3 , 711-719.

TAŞTEMEL ÖZTÜRK, T., CANPOLAT, N., SAYGILI, S. K., BAYRAKCİ, U. S., Soylemezoglu, O., ÖZALTIN, F., ... TOPALOĞLU, R.(2023). A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature. PEDIATRIC NEPHROLOGY , vol.38, no.3, 711-719.

TAŞTEMEL ÖZTÜRK, TUĞBA Et Al. "A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature," PEDIATRIC NEPHROLOGY , vol.38, no.3, 711-719, 2023

TAŞTEMEL ÖZTÜRK, TUĞBA T. Et Al. "A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature." PEDIATRIC NEPHROLOGY , vol.38, no.3, pp.711-719, 2023

TAŞTEMEL ÖZTÜRK, T. Et Al. (2023) . "A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature." PEDIATRIC NEPHROLOGY , vol.38, no.3, pp.711-719.

@article{article, author={TUĞBA TAŞTEMEL ÖZTÜRK Et Al. }, title={A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature}, journal={PEDIATRIC NEPHROLOGY}, year=2023, pages={711-719} }