(Q56863982)

English

Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathy

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Statements

Identification of a novel compound heterozygote SCO2 mutation in cytochrome c oxidase deficient fatal infantile cardioencephalomyopathy (English)
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M Knuf
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J Faber
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R G Huth
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P Freisinger
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F Zepp
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C Kampmann
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January 2007
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96
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1
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130-132
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