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American Journal of Human Genetics|August 26, 2014
A mutation of COX6A1 causes a recessive axonal or mixed form of Charcot-Marie-Tooth diseaseGen Tamiya, Satoshi Makino, Makiko Hayashi, et al.JAMA Neurology|June 21, 2016
Clinical Phenotype and Segregation of Mitochondrial 3243A>G Mutation in 2 Pairs of Monozygotic TwinsKengo Maeda, Hiromichi Kawai, Mitsuru Sanada, et al.Pageof 6