APA (7th ed.) Citation

Chiang, P., Wang, J., Chen, Y., Fu, Q., Zhong, J., Chen, Y., . . . Qi, M. (2012). Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis. Nature genetics, 44(9), 972-974. https://doi.org/10.1038/ng.2370

Chicago Style (17th ed.) Citation

Chiang, Pei-Wen, et al. "Exome Sequencing Identifies NMNAT1 Mutations as a Cause of Leber Congenital Amaurosis." Nature Genetics 44, no. 9 (2012): 972-974. https://doi.org/10.1038/ng.2370.

MLA (9th ed.) Citation

Chiang, Pei-Wen, et al. "Exome Sequencing Identifies NMNAT1 Mutations as a Cause of Leber Congenital Amaurosis." Nature Genetics, vol. 44, no. 9, 2012, pp. 972-974, https://doi.org/10.1038/ng.2370.