Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

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Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2069-2077

Oxford University Press

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The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level

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Human Genetics, Vol. 124, Iss. 1, 2008-08 ,pp. : 43-56

Springer Publishing Company

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Functional Correction of Short-Chain Acyl-CoA Dehydrogenase Deficiency in Transgenic Mice: Implications for Gene Therapy of Human Mitochondrial Enzyme Deficiencies

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Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1451-1455

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Identification of Two Mutations in a Compound Heterozygous Child with Dihydrolipoamide Dehydrogenase Deficiency

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Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders

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