APA (7th ed.) Citation

Hunt, D., Leventer, R. J., Simons, C., Taft, R., Swoboda, K. J., Gawne-Cain, M., . . . Baralle, D. (2014). Whole exome sequencing in family trios reveals de novo mutations in PURA as a cause of severe neurodevelopmental delay and learning disability. Journal of medical genetics, 51(12), 806-813. https://doi.org/10.1136/jmedgenet-2014-102798

Chicago Style (17th ed.) Citation

Hunt, David, Richard J. Leventer, Cas Simons, Ryan Taft, Kathryn J. Swoboda, Mary Gawne-Cain, Alex C. Magee, Peter D. Turnpenny, and Diana Baralle. "Whole Exome Sequencing in Family Trios Reveals De Novo Mutations in PURA as a Cause of Severe Neurodevelopmental Delay and Learning Disability." Journal of Medical Genetics 51, no. 12 (2014): 806-813. https://doi.org/10.1136/jmedgenet-2014-102798.

MLA (9th ed.) Citation

Hunt, David, et al. "Whole Exome Sequencing in Family Trios Reveals De Novo Mutations in PURA as a Cause of Severe Neurodevelopmental Delay and Learning Disability." Journal of Medical Genetics, vol. 51, no. 12, 2014, pp. 806-813, https://doi.org/10.1136/jmedgenet-2014-102798.