1. Poulter, James A, Al-Araimi, Musallam, Conte, Ivan, Inglehearn, Chris F, Toomes, Carmel. 2013. Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism. In American journal of human genetics, 93, 1143-50. doi:10.1016/j.ajhg.2013.11.002. https://pubmed.ncbi.nlm.nih.gov/24290379/
2. Weiner, Chen, Hecht, Idan, Rotenstreich, Ygal, Shomron, Noam, Pras, Eran. 2020. The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus. In Experimental eye research, 193, 107958. doi:10.1016/j.exer.2020.107958. https://pubmed.ncbi.nlm.nih.gov/32032626/
3. Kuht, Helen J, Han, Jinu, Maconachie, Gail D E, Lim, Hyun Taek, Thomas, Mervyn G. . SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. In Human molecular genetics, 29, 2989-3002. doi:10.1093/hmg/ddaa166. https://pubmed.ncbi.nlm.nih.gov/32744312/
4. Liao, Shu-Yi, Lin, Xihong, Christiani, David C. 2013. Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. In Environmental health : a global access science source, 12, 101. doi:10.1186/1476-069X-12-101. https://pubmed.ncbi.nlm.nih.gov/24289273/
5. Schiff, Elena R, Tailor, Vijay K, Chan, Hwei Wuen, Webster, Andrew R, Moosajee, Mariya. 2021. Novel Biallelic Variants and Phenotypic Features in Patients with SLC38A8-Related Foveal Hypoplasia. In International journal of molecular sciences, 22, . doi:10.3390/ijms22031130. https://pubmed.ncbi.nlm.nih.gov/33498813/