APA (7th ed.) Citation

S, S., G, Y., Y, L., J, A., HM, B., B, F., . . . K, B. (2023). The genetic spectrum of congenital ocular motor apraxia type Cogan: An observational study, continued. Orphanet journal of rare diseases, 18(1), 101. https://doi.org/10.1186/s13023-023-02706-5

Chicago Style (17th ed.) Citation

S, Schröder, 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): 101. https://doi.org/10.1186/s13023-023-02706-5.

MLA (9th ed.) Citation

S, Schröder, 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. 101, https://doi.org/10.1186/s13023-023-02706-5.