MITOMAP References for RNA Mutation C602T

• Sakiyama, Y., Okamoto, Y., Higuchi, I., Inamori, Y., Sangatsuda, Y., Michizono, K., Watanabe, O., Hatakeyama, H., Goto, Y., Arimura, K., Takashima, H. (2011) A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy Acta Neuropathologica (Berlin) . 121 (6): 775-783 .