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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External Links
| (P356) |
10.1038/15513
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| (P698) |
10545952
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| (P3181) |
1474515
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| (P5875) |
12754771
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| (P6179) |
1003664613
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