APA (7th ed.) Citation

Dorboz, I., Aiello, C., Simons, C., Stone, R. T., Niceta, M., Elmaleh, M., . . . Bertini, E. (2017). Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy. Brain (London, England : 1878), 140(10), 2550-2556. https://doi.org/10.1093/brain/awx207

Chicago Style (17th ed.) Citation

Dorboz, Imen, et al. "Biallelic Mutations in the Homeodomain of NKX6-2 Underlie a Severe Hypomyelinating Leukodystrophy." Brain (London, England : 1878) 140, no. 10 (2017): 2550-2556. https://doi.org/10.1093/brain/awx207.

MLA (9th ed.) Citation

Dorboz, Imen, et al. "Biallelic Mutations in the Homeodomain of NKX6-2 Underlie a Severe Hypomyelinating Leukodystrophy." Brain (London, England : 1878), vol. 140, no. 10, 2017, pp. 2550-2556, https://doi.org/10.1093/brain/awx207.