SS, K., J, G., MH, M., S, E., & K, V. (2013). Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion. Experimental eye research, 116, 371. https://doi.org/10.1016/j.exer.2013.09.019
Chicago Style (17th ed.) CitationSS, Kumari, Gandhi J, Mustehsan MH, Eren S, and Varadaraj K. "Functional Characterization of an AQP0 Missense Mutation, R33C, That Causes Dominant Congenital Lens Cataract, Reveals Impaired Cell-to-cell Adhesion." Experimental Eye Research 116 (2013): 371. https://doi.org/10.1016/j.exer.2013.09.019.
MLA (9th ed.) CitationSS, Kumari, et al. "Functional Characterization of an AQP0 Missense Mutation, R33C, That Causes Dominant Congenital Lens Cataract, Reveals Impaired Cell-to-cell Adhesion." Experimental Eye Research, vol. 116, 2013, p. 371, https://doi.org/10.1016/j.exer.2013.09.019.