1. Oikarainen, Jaakko, Hinttala, Reetta, Nayebzadeh, Naemeh, Suo-Palosaari, Maria, Uusimaa, Johanna. 2025. Novel intronic variant in NDUFS7 gene results in mitochondrial complex I assembly defect with early basal ganglia and midbrain involvement with progressive neuroimaging findings. In Mitochondrion, , 102007. doi:10.1016/j.mito.2025.102007. https://pubmed.ncbi.nlm.nih.gov/39894241/
2. Ma, Liang, Zhang, Wen, Tang, Jinsong, Yao, Yong-Gang, Chen, Xiaogang. . No association between genetic polymorphisms of the NDUFS7 gene and schizophrenia in Han Chinese. In Psychiatric genetics, 23, 29-32. doi:10.1097/YPG.0b013e32835862c5. https://pubmed.ncbi.nlm.nih.gov/22935918/
3. Pronicka, Ewa, Piekutowska-Abramczuk, Dorota, Ciara, Elżbieta, Krajewska-Walasek, Małgorzata, Płoski, Rafał. 2016. New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre. In Journal of translational medicine, 14, 174. doi:10.1186/s12967-016-0930-9. https://pubmed.ncbi.nlm.nih.gov/27290639/
4. Lebon, Sophie, Minai, Limor, Chretien, Dominique, Bonnefont, Jean-Paul, Rötig, Agnès. 2007. A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome. In Molecular genetics and metabolism, 92, 104-8. doi:. https://pubmed.ncbi.nlm.nih.gov/17604671/
5. Christen, Matthias, Gregor, Anne, Gutierrez-Quintana, Rodrigo, Zweier, Christiane, Leeb, Tosso. 2024. NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. In Scientific reports, 14, 2975. doi:10.1038/s41598-024-53314-7. https://pubmed.ncbi.nlm.nih.gov/38316835/
6. Rhein, Virginie F, Carroll, Joe, Ding, Shujing, Fearnley, Ian M, Walker, John E. 2016. NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human Complex I. In The Journal of biological chemistry, 291, 14851-60. doi:10.1074/jbc.M116.734970. https://pubmed.ncbi.nlm.nih.gov/27226634/
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