Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy. (Q24534480)
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(P577) Thursday, September 28, 2000
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(P1476) "Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathy" (language: en)
(P2093) I Valnot
S Osmond
N Gigarel
B Mehaye
P Rustin
A Munnich
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