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