APA (7th ed.) Citation

JP, R., AF, T., D, H., B, C., L, O., C, B., . . . F, U. (2026). Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy. Orphanet journal of rare diseases, 21(1), . https://doi.org/10.1186/s13023-026-04348-9

Chicago Style (17th ed.) Citation

JP, Roberts, Tang AF, Hernandez D, Carman B, Oiknine L, Brown C, Hurst S, Tang Y, and Urano F. "Natural History of 15 Patients with Autosomal Dominant WFS1 Pathogenic Variants Associated with Sensorineural Hearing Loss and Optic Atrophy." Orphanet Journal of Rare Diseases 21, no. 1 (2026). https://doi.org/10.1186/s13023-026-04348-9.

MLA (9th ed.) Citation

JP, Roberts, et al. "Natural History of 15 Patients with Autosomal Dominant WFS1 Pathogenic Variants Associated with Sensorineural Hearing Loss and Optic Atrophy." Orphanet Journal of Rare Diseases, vol. 21, no. 1, 2026, https://doi.org/10.1186/s13023-026-04348-9.