APA (7th ed.) Citation

Rutsch, F., MacDougall, M., Lu, C., Buers, I., Mamaeva, O., Nitschke, Y., . . . Hennekam, R. (2015). A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome. American journal of human genetics, 96(2), 275-282. https://doi.org/10.1016/j.ajhg.2014.12.014

Chicago Style (17th ed.) Citation

Rutsch, Frank, et al. "A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome." American Journal of Human Genetics 96, no. 2 (2015): 275-282. https://doi.org/10.1016/j.ajhg.2014.12.014.

MLA (9th ed.) Citation

Rutsch, Frank, et al. "A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome." American Journal of Human Genetics, vol. 96, no. 2, 2015, pp. 275-282, https://doi.org/10.1016/j.ajhg.2014.12.014.