1. Abu Hanna, Firas, Zehavi, Yoav, Cohen-Barak, Eran, Rodenburg, Richard J, Spiegel, Ronen. 2024. Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality. In Orphanet journal of rare diseases, 19, 92. doi:10.1186/s13023-024-03094-0. https://pubmed.ncbi.nlm.nih.gov/38419071/
2. Zhuang, Xianbo, Zhang, Guifeng, Bao, Mengxin, Wang, Zheng, Sun, Xiujuan. 2023. Development of a novel immune infiltration-related diagnostic model for Alzheimer's disease using bioinformatic strategies. In Frontiers in immunology, 14, 1147501. doi:10.3389/fimmu.2023.1147501. https://pubmed.ncbi.nlm.nih.gov/37545529/
3. Zou, Kang, Gao, Pengxiang, Xu, Xinping, Zhang, Wei, Zeng, Zhenguo. 2023. Upregulation of NDUFAF2 in Lung Adenocarcinoma Is a Novel Independent Prognostic Biomarker. In Computational and mathematical methods in medicine, 2023, 2912968. doi:10.1155/2023/2912968. https://pubmed.ncbi.nlm.nih.gov/36703939/
4. Janssen, Rolf J R J, Distelmaier, Felix, Smeets, Roel, Smeitink, Jan A M, Nijtmans, Leo G J. 2009. Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder. In Human molecular genetics, 18, 3365-74. doi:10.1093/hmg/ddp276. https://pubmed.ncbi.nlm.nih.gov/19525295/
5. Yin, Kang-Fu, Chen, Ting, Gu, Xiao-Jing, Chi, Li-Yi, Chen, Yong-Ping. 2024. Identification of Potential Causal Genes for Neurodegenerative Diseases by Mitochondria-Related Genome-Wide Mendelian Randomization. In Molecular neurobiology, 62, 3892-3902. doi:10.1007/s12035-024-04528-3. https://pubmed.ncbi.nlm.nih.gov/39347895/
6. Hoefs, Saskia J G, Dieteren, Cindy E J, Rodenburg, Richard J, Nijtmans, Leo G, van den Heuvel, Lambert P. . Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency. In Human mutation, 30, E728-36. doi:10.1002/humu.21037. https://pubmed.ncbi.nlm.nih.gov/19384974/
智鼠故事 
