APA (7th ed.) Citation

Cousin, M., Conboy, E., Wang, J., Lenz, D., Schwab, T. L., Williams, M., . . . Klee, E. W. (2019). RINT1 bi-allelic variations cause infantile-onset recurrent acute liver failure and skeletal abnormalities. The American journal of human genetics, 105(1), . https://doi.org/10.1016/j.ajhg.2019.05.011

Chicago Style (17th ed.) Citation

Cousin, Margot, et al. "RINT1 Bi-allelic Variations Cause Infantile-onset Recurrent Acute Liver Failure and Skeletal Abnormalities." The American Journal of Human Genetics 105, no. 1 (2019). https://doi.org/10.1016/j.ajhg.2019.05.011.

MLA (9th ed.) Citation

Cousin, Margot, et al. "RINT1 Bi-allelic Variations Cause Infantile-onset Recurrent Acute Liver Failure and Skeletal Abnormalities." The American Journal of Human Genetics, vol. 105, no. 1, 2019, https://doi.org/10.1016/j.ajhg.2019.05.011.