1. Drovandi, Stefania, Lipska-Ziętkiewicz, Beata S, Ozaltin, Fatih, Ariceta, Gema, Schaefer, Franz. 2022. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy. In Kidney international, 102, 592-603. doi:10.1016/j.kint.2022.02.040. https://pubmed.ncbi.nlm.nih.gov/35483523/
2. Cao, Q, Li, G M, Xu, H, Zhai, Y H, Wu, B B. . [Coenzyme Q(10) treatment for one child with COQ6 gene mutation induced nephrotic syndrome and literature review]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 55, 135-138. doi:10.3760/cma.j.issn.0578-1310.2017.02.016. https://pubmed.ncbi.nlm.nih.gov/28173653/
3. Doimo, Mara, Trevisson, Eva, Airik, Rannar, Pierrel, Fabien, Salviati, Leonardo. 2013. Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency. In Biochimica et biophysica acta, 1842, 1-6. doi:10.1016/j.bbadis.2013.10.007. https://pubmed.ncbi.nlm.nih.gov/24140869/
4. Justine Perrin, R, Rousset-Rouvière, Caroline, Garaix, Florentine, Boyer, Olivia, Tsimaratos, Michel. 2020. COQ6 mutation in patients with nephrotic syndrome, sensorineural deafness, and optic atrophy. In JIMD reports, 54, 37-44. doi:10.1002/jmd2.12068. https://pubmed.ncbi.nlm.nih.gov/32685349/
5. Nakanishi, Keita, Okamoto, Takayuki, Nozu, Kandai, Ariga, Tadashi, Iijima, Kazumoto. 2018. Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene. In Clinical and experimental nephrology, 23, 669-675. doi:10.1007/s10157-018-1682-z. https://pubmed.ncbi.nlm.nih.gov/30584653/
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