HJ, K., J, H., GDE, M., SE, P., ST, L., R, M., . . . MG, T. (2020). SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. Human molecular genetics, 29(18), 2989. https://doi.org/10.1093/hmg/ddaa166
Chicago Style (17th ed.) CitationHJ, Kuht, et al. "SLC38A8 Mutations Result in Arrested Retinal Development with Loss of Cone Photoreceptor Specialization." Human Molecular Genetics 29, no. 18 (2020): 2989. https://doi.org/10.1093/hmg/ddaa166.
MLA (9th ed.) CitationHJ, Kuht, et al. "SLC38A8 Mutations Result in Arrested Retinal Development with Loss of Cone Photoreceptor Specialization." Human Molecular Genetics, vol. 29, no. 18, 2020, p. 2989, https://doi.org/10.1093/hmg/ddaa166.
Warning: These citations may not always be 100% accurate.