1. Wong-Riley, M, Guo, A, Bachman, N J, Lomax, M I. . Human COX6A1 gene: promoter analysis, cDNA isolation and expression in the monkey brain. In Gene, 247, 63-75. doi:. https://pubmed.ncbi.nlm.nih.gov/10773445/
2. Dong, Hai-Lin, Ma, Yin, Yu, Hao, Bai, Ge, Wu, Zhi-Ying. . Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy. In Brain : a journal of neurology, 144, 2457-2470. doi:10.1093/brain/awab135. https://pubmed.ncbi.nlm.nih.gov/33751098/
3. Tamiya, Gen, Makino, Satoshi, Hayashi, Makiko, Onodera, Osamu, Hayasaka, Kiyoshi. 2014. A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth disease. In American journal of human genetics, 95, 294-300. doi:10.1016/j.ajhg.2014.07.013. https://pubmed.ncbi.nlm.nih.gov/25152455/
4. Li, Fengji, Qiu, Lin, Gao, Qian, Xue, Zhijun, Tao, Anqi. 2023. Comprehensive bioinformatics analysis combined with experimental validation to screen biomarkers for malignant transformation of oral leukoplakia. In Genomics, 115, 110686. doi:10.1016/j.ygeno.2023.110686. https://pubmed.ncbi.nlm.nih.gov/37454941/
5. Santos-Silva, Thamyris, Hazar Ülgen, Doğukan, Lopes, Caio Fábio Baeta, Sandi, Carmen, Gomes, Felipe V. 2023. Transcriptomic analysis reveals mitochondrial pathways associated with distinct adolescent behavioral phenotypes and stress response. In Translational psychiatry, 13, 351. doi:10.1038/s41398-023-02648-3. https://pubmed.ncbi.nlm.nih.gov/37978166/
6. Zhang, Sen, Geng, Yifan, Jiang, Xing, Tian, Xuewen, Wang, Qinglu. 2024. Investigating the mechanisms of inflammation and immune alterations in Parkinson's disease using spatial transcriptomics techniques. In Brain research bulletin, 217, 111076. doi:10.1016/j.brainresbull.2024.111076. https://pubmed.ncbi.nlm.nih.gov/39306046/
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