1. Zhang, Zhihua, Yu, Ran, Shi, Qiuwen, Sang, Qing, Wang, Lei. 2024. COX15 deficiency causes oocyte ferroptosis. In Proceedings of the National Academy of Sciences of the United States of America, 121, e2406174121. doi:10.1073/pnas.2406174121. https://pubmed.ncbi.nlm.nih.gov/39471219/
2. Galvão de Oliveira, Manuella, Tengan, Célia, Micheletti, Cecília, Falconi, Ariane, Perrone, Eduardo. 2021. A novel variant in the COX15 gene causing a fatal infantile cardioencephalomyopathy: A case report with clinical and molecular review. In European journal of medical genetics, 64, 104195. doi:10.1016/j.ejmg.2021.104195. https://pubmed.ncbi.nlm.nih.gov/33746038/
3. Alfadhel, Majid, Lillquist, Yolanda P, Waters, Paula J, Shoffner, John, Vallance, Hilary D. 2011. Infantile cardioencephalopathy due to a COX15 gene defect: report and review. In American journal of medical genetics. Part A, 155A, 840-4. doi:10.1002/ajmg.a.33881. https://pubmed.ncbi.nlm.nih.gov/21412973/
4. Zhang, Cong, Li, Ning, Liu, Ying-Ying, Yang, Song, Wang, Xiang-Peng. 2021. Cox15 is a novel oncogene that required for lung cancer cell proliferation. In Biochemical and biophysical research communications, 578, 70-76. doi:10.1016/j.bbrc.2021.09.010. https://pubmed.ncbi.nlm.nih.gov/34547626/
5. Miryounesi, Mohammad, Fardaei, Majid, Tabei, Seyed Mohammadbagher, Ghafouri-Fard, Soudeh. . Leigh syndrome associated with a novel mutation in the COX15 gene. In Journal of pediatric endocrinology & metabolism : JPEM, 29, 741-4. doi:10.1515/jpem-2015-0396. https://pubmed.ncbi.nlm.nih.gov/26959537/