APA (7th ed.) Citation

AE, O., MV, G., MF, O., SM, R., E, H., D, G., . . . PB, A. (2019). Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. PLoS genetics, 15(2), e1007917. https://doi.org/10.1371/journal.pgen.1007917

Chicago Style (17th ed.) Citation

AE, O'Connell, et al. "Mammalian Hbs1L Deficiency Causes Congenital Anomalies and Developmental Delay Associated with Pelota Depletion and 80S Monosome Accumulation." PLoS Genetics 15, no. 2 (2019): e1007917. https://doi.org/10.1371/journal.pgen.1007917.

MLA (9th ed.) Citation

AE, O'Connell, et al. "Mammalian Hbs1L Deficiency Causes Congenital Anomalies and Developmental Delay Associated with Pelota Depletion and 80S Monosome Accumulation." PLoS Genetics, vol. 15, no. 2, 2019, p. e1007917, https://doi.org/10.1371/journal.pgen.1007917.