APA (7th ed.) Citation

Olinger, E., Alawi, I. A., Al Riyami, M. S., Salmi, I. A., Molinari, E., Faqeih, E. A., . . . Sayer, J. A. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human mutation, 42(10), 1221-1228. https://doi.org/10.1002/humu.24251

Chicago Style (17th ed.) Citation

Olinger, Eric, et al. "A Discarded Synonymous Variant in NPHP3 Explains Nephronophthisis and Congenital Hepatic Fibrosis in Several Families." Human Mutation 42, no. 10 (2021): 1221-1228. https://doi.org/10.1002/humu.24251.

MLA (9th ed.) Citation

Olinger, Eric, et al. "A Discarded Synonymous Variant in NPHP3 Explains Nephronophthisis and Congenital Hepatic Fibrosis in Several Families." Human Mutation, vol. 42, no. 10, 2021, pp. 1221-1228, https://doi.org/10.1002/humu.24251.