APA (7th ed.) Citation

I, A., K, A., TM, J., M, J., SM, B., H, E., . . . N, T. (2025). A novel indel CYP1B1 variant in a large multigenerational Pakistani family expands the mutation spectrum of primary congenital glaucoma. Molecular biology reports, 53(1), 11. https://doi.org/10.1007/s11033-025-11109-7

Chicago Style (17th ed.) Citation

I, Anjum, Aslam K, Jamil TM, John M, Baig SM, Eiberg H, Hansen L, and Tommerup N. "A Novel Indel CYP1B1 Variant in a Large Multigenerational Pakistani Family Expands the Mutation Spectrum of Primary Congenital Glaucoma." Molecular Biology Reports 53, no. 1 (2025): 11. https://doi.org/10.1007/s11033-025-11109-7.

MLA (9th ed.) Citation

I, Anjum, et al. "A Novel Indel CYP1B1 Variant in a Large Multigenerational Pakistani Family Expands the Mutation Spectrum of Primary Congenital Glaucoma." Molecular Biology Reports, vol. 53, no. 1, 2025, p. 11, https://doi.org/10.1007/s11033-025-11109-7.