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. Kloth, Katja, Synofzik, Matthis, Kernstock, Christoph, Wissinger, Bernd, Weisschuh, Nicole. 2019. Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports. In BMC medical genetics, 20, 62. doi:10.1186/s12881-019-0795-x. https://pubmed.ncbi.nlm.nih.gov/30961538/
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. Désir, Julie, Coppieters, Frauke, Van Regemorter, Nicole, Abramowicz, Marc, Cordonnier, Monique. 2012. TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy. In Molecular vision, 18, 1849-57. doi:. https://pubmed.ncbi.nlm.nih.gov/22815638/
6. Rocatcher, Aude, Desquiret-Dumas, Valérie, Charif, Majida, Reynier, Pascal, Amati-Bonneau, Patrizia. . The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands. In Brain : a journal of neurology, 146, 455-460. doi:10.1093/brain/awac395. https://pubmed.ncbi.nlm.nih.gov/36317462/
7. 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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