A case of Ohtahara syndrome with cytochrome oxidase deficiency
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[1] V. Salas,et al. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria , 1996, Nature Genetics.
[2] S. Dimauro,et al. Reversible mitochondrial myopathy with cytochrome c oxidase deficiency. , 1992, Archives of disease in childhood.
[3] M. Clarke,et al. EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY WITH SUPPRESSION BURST: OHTAHARA SYNDROME , 1987, Developmental medicine and child neurology.
[4] S. Ohtahara. Early-infantile epileptic encephalopathy with suppression-bursts , 1992 .
[5] R. Capaldi,et al. Structure and function of cytochrome c oxidase. , 1990, Annual review of biochemistry.