APA (7th ed.) Citation

Cannata Serio, M., Graham, L. A., Ashikov, A., Larsen, L. E., Raymond, K., Timal, S., . . . Lefeber, D. J. (2020). Mutations in the V-ATPase assembly factor VMA21 cause a congenital disorder of glycosylation with autophagic liver disease. Hepatology, 72(6), . https://doi.org/10.1002/hep.31218

Chicago Style (17th ed.) Citation

Cannata Serio, Magda, et al. "Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation with Autophagic Liver Disease." Hepatology 72, no. 6 (2020). https://doi.org/10.1002/hep.31218.

MLA (9th ed.) Citation

Cannata Serio, Magda, et al. "Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation with Autophagic Liver Disease." Hepatology, vol. 72, no. 6, 2020, https://doi.org/10.1002/hep.31218.