Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.
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Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy.
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(P356) |
10.1086/321202
10.1016/S0002-9297(07)62940-1 |
(P698) |
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(P932) |
1288552
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(P8608) |
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