APA (7th ed.) Citation

Johnson, J. O., Gibbs, J. R., Megarbane, A., Urtizberea, J. A., Hernandez, D. G., Foley, A. R., . . . Singleton, A. B. (2012). Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. Brain (London, England : 1878), 135(9), 2875-2882. https://doi.org/10.1093/brain/aws161

Chicago Style (17th ed.) Citation

Johnson, Janel O., et al. "Exome Sequencing Reveals Riboflavin Transporter Mutations as a Cause of Motor Neuron Disease." Brain (London, England : 1878) 135, no. 9 (2012): 2875-2882. https://doi.org/10.1093/brain/aws161.

MLA (9th ed.) Citation

Johnson, Janel O., et al. "Exome Sequencing Reveals Riboflavin Transporter Mutations as a Cause of Motor Neuron Disease." Brain (London, England : 1878), vol. 135, no. 9, 2012, pp. 2875-2882, https://doi.org/10.1093/brain/aws161.