APA (7th ed.) Citation

Weisschuh, N., Sturm, M., Baumann, B., Audo, I., Ayuso, C., Bocquet, B., . . . Kohl, S. (2020). Deep‐intronic variants in CNGB3 cause achromatopsia by pseudoexon activation. Human mutation, 41(1), 255-264. https://doi.org/10.1002/humu.23920

Chicago Style (17th ed.) Citation

Weisschuh, Nicole, et al. "Deep‐intronic Variants in CNGB3 Cause Achromatopsia by Pseudoexon Activation." Human Mutation 41, no. 1 (2020): 255-264. https://doi.org/10.1002/humu.23920.

MLA (9th ed.) Citation

Weisschuh, Nicole, et al. "Deep‐intronic Variants in CNGB3 Cause Achromatopsia by Pseudoexon Activation." Human Mutation, vol. 41, no. 1, 2020, pp. 255-264, https://doi.org/10.1002/humu.23920.