1. Kim, Eun-Cheol, Moon, Ji-Hoi, Kang, Sang W, Kwon, Byungsuk, Lee, Hyeon-Woo. 2014. TMEM126A, a CD137 ligand binding protein, couples with the TLR4 signal transduction pathway in macrophages. In Molecular immunology, 64, 244-51. doi:10.1016/j.molimm.2014.12.001. https://pubmed.ncbi.nlm.nih.gov/25549946/
2. Hanein, Sylvain, Garcia, Mathilde, Fares-Taie, Lucas, Devaux, Frédéric, Rozet, Jean-Michel. 2013. TMEM126A is a mitochondrial located mRNA (MLR) protein of the mitochondrial inner membrane. In Biochimica et biophysica acta, 1830, 3719-33. doi:10.1016/j.bbagen.2013.02.025. https://pubmed.ncbi.nlm.nih.gov/23500070/
3. D'Angelo, Luigi, Astro, Elisa, De Luise, Monica, Fernandez-Vizarra, Erika, Iommarini, Luisa. . NDUFS3 depletion permits complex I maturation and reveals TMEM126A/OPA7 as an assembly factor binding the ND4-module intermediate. In Cell reports, 35, 109002. doi:10.1016/j.celrep.2021.109002. https://pubmed.ncbi.nlm.nih.gov/33882309/
4. Hanein, Sylvain, Perrault, Isabelle, Roche, Olivier, Kaplan, Josseline, Rozet, Jean-Michel. 2009. TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive nonsyndromic optic atrophy. In American journal of human genetics, 84, 493-8. doi:10.1016/j.ajhg.2009.03.003. https://pubmed.ncbi.nlm.nih.gov/19327736/
5. Meyer, Esther, Michaelides, Michel, Tee, Louise J, Moore, Anthony T, Maher, Eamonn R. 2010. Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy. In Molecular vision, 16, 650-64. doi:. https://pubmed.ncbi.nlm.nih.gov/20405026/
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