APA (7th ed.) Citation

GR, W., JC, S., C, M., M, G., CA, G., JR, R., . . . PJ, L. (2014). Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology. American journal of human genetics, 95(6), 729. https://doi.org/10.1016/j.ajhg.2014.10.015

Chicago Style (17th ed.) Citation

GR, Wilson, et al. "Mutations in RAB39B Cause X-linked Intellectual Disability and Early-onset Parkinson Disease with α-synuclein Pathology." American Journal of Human Genetics 95, no. 6 (2014): 729. https://doi.org/10.1016/j.ajhg.2014.10.015.

MLA (9th ed.) Citation

GR, Wilson, et al. "Mutations in RAB39B Cause X-linked Intellectual Disability and Early-onset Parkinson Disease with α-synuclein Pathology." American Journal of Human Genetics, vol. 95, no. 6, 2014, p. 729, https://doi.org/10.1016/j.ajhg.2014.10.015.