APA (7th ed.) Citation

Huppke, P., Brendel, C., Kalscheuer, V., Korenke, G., Marquardt, I., Freisinger, P., . . . Gärtner, J. (2012). Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin. American journal of human genetics, 90(1), 61-68. https://doi.org/10.1016/j.ajhg.2011.11.030

Chicago Style (17th ed.) Citation

Huppke, Peter, et al. "Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin." American Journal of Human Genetics 90, no. 1 (2012): 61-68. https://doi.org/10.1016/j.ajhg.2011.11.030.

MLA (9th ed.) Citation

Huppke, Peter, et al. "Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin." American Journal of Human Genetics, vol. 90, no. 1, 2012, pp. 61-68, https://doi.org/10.1016/j.ajhg.2011.11.030.