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HARVARD Citation
Jaksch, M. et al. (1998). A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.. Journal of medical genetics. 35 (11), pp. 895-900. [Online].