Citations for
1EEF2, SCA26
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.
Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM.
Hum Mol Genet 21(26):5472-83. doi: 10.1093/hmg/dds392. Epub 2012 Sep 21. 2012
2SCA26
Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
Yu GY, Howell MJ, Roller MJ, Xie TD, Gomez CM.
Ann Neurol 57(3):349-54. 2005