Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood (Q24303615)

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Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood
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    Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood (English)
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    A W Strauss
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    C K Powell
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    D E Hale
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    M M Anderson
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    A Ahuja
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    J C Brackett
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    H F Sims
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    7 November 1995
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    92
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    23
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    10496-500
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