1. Poduri, Annapurna, Heinzen, Erin L, Chitsazzadeh, Vida, Salih, Mustafa A, Walsh, Christopher A. . SLC25A22 is a novel gene for migrating partial seizures in infancy. In Annals of neurology, 74, 873-82. doi:10.1002/ana.23998. https://pubmed.ncbi.nlm.nih.gov/24596948/
2. Wong, Chi Chun, Qian, Yun, Li, Xiaona, Cai, Zongwei, Yu, Jun. 2016. SLC25A22 Promotes Proliferation and Survival of Colorectal Cancer Cells With KRAS Mutations and Xenograft Tumor Progression in Mice via Intracellular Synthesis of Aspartate. In Gastroenterology, 151, 945-960.e6. doi:10.1053/j.gastro.2016.07.011. https://pubmed.ncbi.nlm.nih.gov/27451147/
3. Cohen, Rony, Basel-Vanagaite, Lina, Goldberg-Stern, Hadassah, Behar, Doron M, Straussberg, Rachel. 2014. Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22. In European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 18, 801-5. doi:10.1016/j.ejpn.2014.06.007. https://pubmed.ncbi.nlm.nih.gov/25033742/
4. André, M-V, Cacciagli, P, Cano, A, Villard, L, Milh, M. 2020. The phenotype caused by recessive variations in SLC25A22: Report of a new case and literature review. In Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 28, 87-92. doi:10.1016/j.arcped.2020.10.015. https://pubmed.ncbi.nlm.nih.gov/33342683/