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-referens (17:e uppl.)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-referens (9:e uppl.)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.
