Kılıç, R. K. Et Al. 2023. Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease (PP-033). 24. Ulusal Çocuk Nörolojisi Kongresi , (Muğla, Turkey), 187.

Kılıç, R. K., Hırfanoğlu, T., Kayhan, G., Demir, E., & Arhan, E., (2023). Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease (PP-033) . 24. Ulusal Çocuk Nörolojisi Kongresi (pp.187). Muğla, Turkey

Kılıç, RECEP Et Al. "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease (PP-033)," 24. Ulusal Çocuk Nörolojisi Kongresi , Muğla, Turkey, 2023

Kılıç, RECEP K. Et Al. "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease (PP-033)." 24. Ulusal Çocuk Nörolojisi Kongresi , Muğla, Turkey, pp.187, 2023

Kılıç, R. K. Et Al. (2023) . "Late Onset Cerebral Folate Transporter Deficiency with a Novel Mutation Mimicking SSPE and Wilson’s disease (PP-033)." 24. Ulusal Çocuk Nörolojisi Kongresi , Muğla, Turkey, p.187.

@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-033)}, congress name={24. Ulusal Çocuk Nörolojisi Kongresi }, city={Muğla}, country={Turkey}, year={2023}, pages={187} }