APA (7th ed.) Citation

Chograni, M., Alahdal, H. M., & Rejili, M. (2023). Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene. Human genomics, 17(1), 41-9. https://doi.org/10.1186/s40246-023-00492-6

Chicago Style (17th ed.) Citation

Chograni, M., H. M. Alahdal, and M. Rejili. "Autosomal Recessive Congenital Cataract Is Associated with a Novel 4-bp Splicing Deletion Mutation in a Novel C10orf71 Human Gene." Human Genomics 17, no. 1 (2023): 41-9. https://doi.org/10.1186/s40246-023-00492-6.

MLA (9th ed.) Citation

Chograni, M., et al. "Autosomal Recessive Congenital Cataract Is Associated with a Novel 4-bp Splicing Deletion Mutation in a Novel C10orf71 Human Gene." Human Genomics, vol. 17, no. 1, 2023, pp. 41-9, https://doi.org/10.1186/s40246-023-00492-6.