APA (7th ed.) Citation

Tezen, D., Şimşir, G., Çokar, Ö., Demirbilek, V., Başak, A. N., & Yapıcı, Z. (2022). Four Turkish families with hyperekplexia: A missense mutation and the exon 1–7 deletion in the GLRA1 gene. Parkinsonism & related disorders, 105, 128-131. https://doi.org/10.1016/j.parkreldis.2022.11.011

Chicago Style (17th ed.) Citation

Tezen, Didem, Gülşah Şimşir, Özlem Çokar, Veysi Demirbilek, A. Nazlı Başak, and Zuhal Yapıcı. "Four Turkish Families with Hyperekplexia: A Missense Mutation and the Exon 1–7 Deletion in the GLRA1 Gene." Parkinsonism & Related Disorders 105 (2022): 128-131. https://doi.org/10.1016/j.parkreldis.2022.11.011.

MLA (9th ed.) Citation

Tezen, Didem, et al. "Four Turkish Families with Hyperekplexia: A Missense Mutation and the Exon 1–7 Deletion in the GLRA1 Gene." Parkinsonism & Related Disorders, vol. 105, 2022, pp. 128-131, https://doi.org/10.1016/j.parkreldis.2022.11.011.