A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease (Q24645475)

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A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease
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    A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease (English)
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    Andrew J Duncan
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    Harry Costello
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    Iain P Hargreaves
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    Michio Hirano
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    Catarina M Quinzii
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    Peter T Clayton
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    May 2009
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    84
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    5
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    558-66
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