Kılıç, R. K. Et Al. 2023. Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247). SSIEM Annual Symposium, Journal of Inherited Metabolic Disese) , (Ashdod, Israel), 247.

Kılıç, R. K., Arhan, E., Kayhan, G., Demir, E., & Hırfanoğlu, T., (2023). Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247) . SSIEM Annual Symposium, Journal of Inherited Metabolic Disese) (pp.247). Ashdod, Israel

Kılıç, RECEP Et Al. "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247)," SSIEM Annual Symposium, Journal of Inherited Metabolic Disese), Ashdod, Israel, 2023

Kılıç, RECEP K. Et Al. "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247)." SSIEM Annual Symposium, Journal of Inherited Metabolic Disese) , Ashdod, Israel, pp.247, 2023

Kılıç, R. K. Et Al. (2023) . "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247)." SSIEM Annual Symposium, Journal of Inherited Metabolic Disese) , Ashdod, Israel, p.247.

@conferencepaper{conferencepaper, author={RECEP KAMİL KILIÇ Et Al. }, title={Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease. (PP-247)}, congress name={SSIEM Annual Symposium, Journal of Inherited Metabolic Disese)}, city={Ashdod}, country={Israel}, year={2023}, pages={247} }