APA (7th ed.) Citation

Schröder, S., Yigit, G., Li, Y., Altmüller, J., Büttel, H., Fiedler, B., . . . Brockmann, K. (2023). The genetic spectrum of congenital ocular motor apraxia type Cogan: An observational study, continued. Orphanet Journal of Rare Diseases, 18(1), 1. https://doi.org/10.1186/s13023-023-02706-5

Chicago Style (17th ed.) Citation

Schröder, Simone, et al. "The Genetic Spectrum of Congenital Ocular Motor Apraxia Type Cogan: An Observational Study, Continued." Orphanet Journal of Rare Diseases 18, no. 1 (2023): 1. https://doi.org/10.1186/s13023-023-02706-5.

MLA (9th ed.) Citation

Schröder, Simone, et al. "The Genetic Spectrum of Congenital Ocular Motor Apraxia Type Cogan: An Observational Study, Continued." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, p. 1, https://doi.org/10.1186/s13023-023-02706-5.