Cite
An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2.
MLA
Cecilia Mancini, et al. “An Atypical Form of AOA2 with Myoclonus Associated with Mutations in SETX and AFG3L2.” BMC Medical Genetics, vol. 16, no. 1, Mar. 2015, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s12881-015-0159-0.
APA
Cecilia Mancini, Laura Orsi, Yiran Guo, Jiankang Li, Yulan Chen, Fengxiang Wang, Lifeng Tian, Xuanzhu Liu, Jianguo Zhang, Hui Jiang, Bruce Shike Nmezi, Takashi Tatsuta, Giorgio, E., Di Gregorio, E., Cavalieri, S., Pozzi, E., Mortara, P., Caglio, M. M., Balducci, A., & Pinessi, L. (2015). An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2. BMC Medical Genetics, 16(1), 1–7. https://doi.org/10.1186/s12881-015-0159-0
Chicago
Cecilia Mancini, Laura Orsi, Yiran Guo, Jiankang Li, Yulan Chen, Fengxiang Wang, Lifeng Tian, et al. 2015. “An Atypical Form of AOA2 with Myoclonus Associated with Mutations in SETX and AFG3L2.” BMC Medical Genetics 16 (1): 1–7. doi:10.1186/s12881-015-0159-0.