APA (7th ed.) Citation

NM, E., CA, T., AF, A., HM, F., DN, B., & ML, E. (2025). A novel founder variant in BEST1 gene causing autosomal recessive bestrophinopathy. Orphanet journal of rare diseases, 20(1), 248. https://doi.org/10.1186/s13023-025-03813-1

Chicago Style (17th ed.) Citation

NM, Elbagoury, Tawfik CA, Abdel-Aleem AF, Fathy HM, Baddar DN, and Essawi ML. "A Novel Founder Variant in BEST1 Gene Causing Autosomal Recessive Bestrophinopathy." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 248. https://doi.org/10.1186/s13023-025-03813-1.

MLA (9th ed.) Citation

NM, Elbagoury, et al. "A Novel Founder Variant in BEST1 Gene Causing Autosomal Recessive Bestrophinopathy." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 248, https://doi.org/10.1186/s13023-025-03813-1.