RAB39B mutations are a rare finding in Parkinson disease patients.

MLA

Löchte, Tobias, et al. “RAB39B Mutations Are a Rare Finding in Parkinson Disease Patients.” Parkinsonism & Related Disorders, vol. 23, Feb. 2016, pp. 116–17. EBSCOhost, https://doi.org/10.1016/j.parkreldis.2015.12.014.

APA

Löchte, T., Brüggemann, N., Vollstedt, E.-J., Krause, P., Domingo, A., Rosales, R., Lee, L. V., Hopfner, F., Westenberger, A., Kühn, A., Klein, C., & Lohmann, K. (2016). RAB39B mutations are a rare finding in Parkinson disease patients. Parkinsonism & Related Disorders, 23, 116–117. https://doi.org/10.1016/j.parkreldis.2015.12.014

Chicago

Löchte, Tobias, Norbert Brüggemann, Eva-Juliane Vollstedt, Patricia Krause, Aloysius Domingo, Raymond Rosales, Lillian V Lee, et al. 2016. “RAB39B Mutations Are a Rare Finding in Parkinson Disease Patients.” Parkinsonism & Related Disorders 23 (February): 116–17. doi:10.1016/j.parkreldis.2015.12.014.