1. Glasgow, Ruth I C, Thompson, Kyle, Barbosa, Inês A, McFarland, Robert, Taylor, Robert W. 2017. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. In Neurogenetics, 18, 227-235. doi:10.1007/s10048-017-0526-4. https://pubmed.ncbi.nlm.nih.gov/29075935/
2. Zhang, Minjie, Hogstrand, Christer, Pontrelli, Paola, Malik, Afshan N. 2024. Co-regulation and synteny of GFM2 and NSA2 links ribosomal function in mitochondria and the cytosol with chronic kidney disease. In Molecular medicine (Cambridge, Mass.), 30, 176. doi:10.1186/s10020-024-00930-8. https://pubmed.ncbi.nlm.nih.gov/39396937/
3. Kistol, Denis, Tsygankova, Polina, Krylova, Tatiana, Migiaev, Ochir, Zakharova, Ekaterina. 2023. Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. In International journal of molecular sciences, 24, . doi:10.3390/ijms24021597. https://pubmed.ncbi.nlm.nih.gov/36675121/
4. Fukumura, Shinobu, Ohba, Chihiro, Watanabe, Toshihide, Matsumoto, Naomichi, Tsutsumi, Hiroyuki. 2015. Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita. In Journal of human genetics, 60, 509-13. doi:10.1038/jhg.2015.57. https://pubmed.ncbi.nlm.nih.gov/26016410/
5. Wei, Chengcheng, Deng, Changqi, Dong, Rui, Hou, Teng, Chen, Zhaohui. 2023. Multi-omics analysis reveals critical metabolic regulators in bladder cancer. In International urology and nephrology, 56, 923-934. doi:10.1007/s11255-023-03841-5. https://pubmed.ncbi.nlm.nih.gov/37882969/
6. Kummer, Eva, Schubert, Katharina Noel, Schoenhut, Tanja, Scaiola, Alain, Ban, Nenad. 2021. Structural basis of translation termination, rescue, and recycling in mammalian mitochondria. In Molecular cell, 81, 2566-2582.e6. doi:10.1016/j.molcel.2021.03.042. https://pubmed.ncbi.nlm.nih.gov/33878294/
7. Hammarsund, M, Wilson, W, Corcoran, M, Grandér, D, Sangfelt, O. 2001. Identification and characterization of two novel human mitochondrial elongation factor genes, hEFG2 and hEFG1, phylogenetically conserved through evolution. In Human genetics, 109, 542-50. doi:. https://pubmed.ncbi.nlm.nih.gov/11735030/
智鼠故事 
