APA (7th ed.) Citation

Pasutto, F., Ekici, A., Reis, A., Kremers, J., & Huchzermeyer, C. (2018). Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy. Ophthalmic Genetics, 39(6), 741. https://doi.org/10.1080/13816810.2018.1520263

Chicago Style (17th ed.) Citation

Pasutto, Francesca, Arif Ekici, André Reis, Jan Kremers, and Cord Huchzermeyer. "Novel Truncating Mutation in CACNA1F in a Young Male Patient Diagnosed with Optic Atrophy." Ophthalmic Genetics 39, no. 6 (2018): 741. https://doi.org/10.1080/13816810.2018.1520263.

MLA (9th ed.) Citation

Pasutto, Francesca, et al. "Novel Truncating Mutation in CACNA1F in a Young Male Patient Diagnosed with Optic Atrophy." Ophthalmic Genetics, vol. 39, no. 6, 2018, p. 741, https://doi.org/10.1080/13816810.2018.1520263.