Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene (Q22010737)

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Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
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    Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene (English)
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    L C Papadopoulou
    November 1999
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    23
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    3
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    333-7
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