1. Wang, Jun Ling, Yang, Xu, Xia, Kun, Li, Rui Qiang, Tang, Bei Sha. 2010. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing. In Brain : a journal of neurology, 133, 3510-8. doi:10.1093/brain/awq323. https://pubmed.ncbi.nlm.nih.gov/21106500/
2. Chen, Yanxing, Wu, Dengchang, Luo, Benyan, Zhao, Guohua, Wang, Kang. 2020. TGM6 L517W is not a pathogenic variant for spinocerebellar ataxia type 35. In Neurology. Genetics, 6, e424. doi:10.1212/NXG.0000000000000424. https://pubmed.ncbi.nlm.nih.gov/32426513/
3. Fung, Jasmine L F, Tsang, Mandy H Y, Leung, Gordon K C, Yu, Mullin H C, Chung, Brian H Y. 2019. A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35. In Parkinsonism & related disorders, 63, 42-45. doi:10.1016/j.parkreldis.2019.01.013. https://pubmed.ncbi.nlm.nih.gov/30670339/
4. Tripathy, Debasmita, Vignoli, Beatrice, Ramesh, Nandini, Pennuto, Maria, Basso, Manuela. . Mutations in TGM6 induce the unfolded protein response in SCA35. In Human molecular genetics, 26, 3749-3762. doi:10.1093/hmg/ddx259. https://pubmed.ncbi.nlm.nih.gov/28934387/