A novel homozygous missense variant in <italic>POC1B</italic> causes cone dystrophy in a consanguineous Pakistani family.

MLA

Munir, Asad, et al. “A Novel Homozygous Missense Variant in POC1B Causes Cone Dystrophy in a Consanguineous Pakistani Family.” Ophthalmic Genetics, Nov. 2024, pp. 1–9. EBSCOhost, https://doi.org/10.1080/13816810.2024.2430700.

APA

Munir, A., Khan, I. U., Rashid, A., Anwar, I., Shah, S., Oreshkov, S., Ullah, M., Khan, H. A., Ullah, U., Ahmad, A., Ansar, M., & Rehman, A. U. (2024). A novel homozygous missense variant in POC1B causes cone dystrophy in a consanguineous Pakistani family. Ophthalmic Genetics, 1–9. https://doi.org/10.1080/13816810.2024.2430700

Chicago

Munir, Asad, Inam Ullah Khan, Abdur Rashid, Ijaz Anwar, Sabawoon Shah, Sergey Oreshkov, Mukhtar Ullah, et al. 2024. “A Novel Homozygous Missense Variant in POC1B Causes Cone Dystrophy in a Consanguineous Pakistani Family.” Ophthalmic Genetics, November, 1–9. doi:10.1080/13816810.2024.2430700.