APA (7th ed.) Citation

Malik, M. A., Saqib, M. A. N., Mientjes, E., Acharya, A., Alam, M. R., Wallaard, I., . . . Ansar, M. (2023). A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome. European Journal of Human Genetics, 31(12), 1447. https://doi.org/10.1038/s41431-023-01475-w

Chicago Style (17th ed.) Citation

Malik, Madiha Amin, et al. "A Loss of Function Variant in AGPAT3 Underlies Intellectual Disability and Retinitis Pigmentosa (IDRP) Syndrome." European Journal of Human Genetics 31, no. 12 (2023): 1447. https://doi.org/10.1038/s41431-023-01475-w.

MLA (9th ed.) Citation

Malik, Madiha Amin, et al. "A Loss of Function Variant in AGPAT3 Underlies Intellectual Disability and Retinitis Pigmentosa (IDRP) Syndrome." European Journal of Human Genetics, vol. 31, no. 12, 2023, p. 1447, https://doi.org/10.1038/s41431-023-01475-w.