1. Petruzzella, Vittoria, Tessa, Alessandra, Torraco, Alessandra, Federico, Antonio, Santorelli, Filippo M. 2007. The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy. In Biochemical and biophysical research communications, 355, 181-7. doi:. https://pubmed.ncbi.nlm.nih.gov/17292333/
2. de Masfrand, Servane, Cogné, Benjamin, Nizon, Mathilde, Piton, Amélie, Isidor, Bertrand. 2024. Penetrance, variable expressivity and monogenic neurodevelopmental disorders. In European journal of medical genetics, 69, 104932. doi:10.1016/j.ejmg.2024.104932. https://pubmed.ncbi.nlm.nih.gov/38453051/
3. Amate-García, Guillermo, Ballesta-Martínez, María Juliana, Serrano-Lorenzo, Pablo, Guillén-Navarro, Encarnación, Martín, Miguel A. 2023. A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. In International journal of molecular sciences, 24, . doi:10.3390/ijms24021743. https://pubmed.ncbi.nlm.nih.gov/36675256/
4. Yang, Yin, Li, Jing-Hui, Yao, Bo-Chen, Wang, Lian-Qun, Guo, Zhi-Gang. 2023. NDUFB11 and NDUFS3 play a role in atherosclerosis and chronic stress. In Aging, 15, 8026-8043. doi:10.18632/aging.204947. https://pubmed.ncbi.nlm.nih.gov/37642954/
5. Gurok, Ulf, Bork, Kaya, Nuber, Ulrike, Nöhring, Sabine, Horstkorte, Rüdiger. 2006. Expression of Ndufb11 encoding the neuronal protein 15.6 during neurite outgrowth and development. In Gene expression patterns : GEP, 7, 370-4. doi:. https://pubmed.ncbi.nlm.nih.gov/16962385/
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7. Reinson, Karit, Kovacs-Nagy, Reka, Õiglane-Shlik, Eve, Rodenburg, Richard J, Õunap, Katrin. 2018. Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11. In European journal of medical genetics, 62, 103572. doi:10.1016/j.ejmg.2018.11.006. https://pubmed.ncbi.nlm.nih.gov/30423443/
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