| 1 | ACADL
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| Mitochondrial dysfunction due to long-chain Acyl-CoA dehydrogenase deficiency causes hepatic steatosis and hepatic insulin resistance.
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| Zhang D, Liu ZX, Choi CS, Tian L, Kibbey R, Dong J, Cline GW, Wood PA, Shulman GI.
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| Proc Natl Acad Sci U S A 104(43):17075-80. Epub 2007 Oct 16. 2007
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| 2 | ACADL
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| Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.
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| Clark-Taylor T, Clark-Taylor BE.
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| Med Hypotheses 62(6):970-5. 2004
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| 3 | ACADL
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| Disrupted blastocoele formation reveals a critical developmental role for long-chain acyl-CoA dehydrogenase.
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| Berger PS, Wood PA.
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| Mol Genet Metab 82(4):266-72. 2004
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| 4 | ACADL
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| Long-chain acyl-CoA dehydrogenase is a key enzyme in the mitochondrial beta-oxidation of unsaturated fatty acids.
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| Lea W, Abbas AS, Sprecher H, Vockley J, Schulz H.
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| Biochim Biophys Acta 1485(2-3):121-8. 2000
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| 5 | ACADVL, ACADL
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| Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.
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| Andresen BS, et al.
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| Hum Mol Genet 5 : 461-472. 1996
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| 6 | ACADL
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| Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2.
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| Indo Y, et al.
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| Genomics 11 : 609-620. 1991
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| 7 | ACADL
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| The molecular basis of human long chain acyl CoA dehydrogenase deficiency.
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| Kelly D, et al.
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| Am J Hum Genet 49S : 409. 1991
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| 8 | ACADL
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| Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase.
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| Wanders RJA, et al.
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| Lancet II : 52-53. 1989
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| 9 | ACADL
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| Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.
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| Hale DE, et al.
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| Pediatr Res 19 : 666-671. 1985
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