Cite
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.
MLA
Daneshmandpour, Yousef, et al. “A Novel Mutation in the ALS2 Gene in an Iranian Kurdish Family with Juvenile Amyotrophic Lateral Sclerosis.” Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, vol. 24, no. 1–2, Feb. 2023, pp. 148–51. EBSCOhost, https://doi.org/10.1080/21678421.2022.2100263.
APA
Daneshmandpour, Y., Bahmanpour, Z., Kazeminasab, S., Aghaei Moghadam, E., Alehabib, E., Chapi, M., Tafakhori, A., Aghaei, N., Darvish, H., & Emamalizadeh, B. (2023). A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 24(1–2), 148–151. https://doi.org/10.1080/21678421.2022.2100263
Chicago
Daneshmandpour, Yousef, Zahra Bahmanpour, Somayeh Kazeminasab, Ehsan Aghaei Moghadam, Elham Alehabib, Marjan Chapi, Abbas Tafakhori, Negar Aghaei, Hossein Darvish, and Babak Emamalizadeh. 2023. “A Novel Mutation in the ALS2 Gene in an Iranian Kurdish Family with Juvenile Amyotrophic Lateral Sclerosis.” Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration 24 (1–2): 148–51. doi:10.1080/21678421.2022.2100263.