APA (7th ed.) Citation

SJ, B., MM, H., LS, S., PF, K., LC, T., AS, K., . . . P, H. (2011). A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement. European journal of human genetics : EJHG, 19(10), 1074. https://doi.org/10.1038/ejhg.2011.86

Chicago Style (17th ed.) Citation

SJ, Bowne, et al. "A Dominant Mutation in RPE65 Identified by Whole-exome Sequencing Causes Retinitis Pigmentosa with Choroidal Involvement." European Journal of Human Genetics : EJHG 19, no. 10 (2011): 1074. https://doi.org/10.1038/ejhg.2011.86.

MLA (9th ed.) Citation

SJ, Bowne, et al. "A Dominant Mutation in RPE65 Identified by Whole-exome Sequencing Causes Retinitis Pigmentosa with Choroidal Involvement." European Journal of Human Genetics : EJHG, vol. 19, no. 10, 2011, p. 1074, https://doi.org/10.1038/ejhg.2011.86.