APA (7th ed.) Citation

Neissi, M., Al-Zaalan, A. R., Mohammadi-Asl, M., Roghani, M., Mohammadi-Asl, J., & Jorfi, K. (2025). ARV1 p.Gln62Ter, a novel mutation linked to developmental and epileptic encephalopathy-38. Journal of Rare Diseases, 4(1), 1. https://doi.org/10.1007/s44162-025-00066-1

Chicago Style (17th ed.) Citation

Neissi, Mostafa, Ayoob Radhi Al-Zaalan, Misagh Mohammadi-Asl, Mojdeh Roghani, Javad Mohammadi-Asl, and Kamele Jorfi. "ARV1 P.Gln62Ter, a Novel Mutation Linked to Developmental and Epileptic Encephalopathy-38." Journal of Rare Diseases 4, no. 1 (2025): 1. https://doi.org/10.1007/s44162-025-00066-1.

MLA (9th ed.) Citation

Neissi, Mostafa, et al. "ARV1 P.Gln62Ter, a Novel Mutation Linked to Developmental and Epileptic Encephalopathy-38." Journal of Rare Diseases, vol. 4, no. 1, 2025, p. 1, https://doi.org/10.1007/s44162-025-00066-1.