Kiratli Nalbant, E. Et Al. 2019. A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene. JAAD Case Reports , vol.5, no.5 , 436-438.

Kiratli Nalbant, E., Karaosmanoglu, N., Kutlu, O., CEYLANER, S., & Eksioglu, H. M., (2019). A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene. JAAD Case Reports , vol.5, no.5, 436-438.

Kiratli Nalbant, Esra Et Al. "A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene," JAAD Case Reports , vol.5, no.5, 436-438, 2019

Kiratli Nalbant, Esra K. Et Al. "A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene." JAAD Case Reports , vol.5, no.5, pp.436-438, 2019

Kiratli Nalbant, E. Et Al. (2019) . "A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene." JAAD Case Reports , vol.5, no.5, pp.436-438.

@article{article, author={Esra Kiratli Nalbant Et Al. }, title={A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the PEPD gene}, journal={JAAD Case Reports}, year=2019, pages={436-438} }