1 | ACAD8, ACAD8D |
Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans. | |
Nguyen TV, Andresen BS, Corydon TJ, Ghisla S, Abd-El Razik N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J. | |
Mol Genet Metab 77(1-2):68-79. 2002 | |
2 | ACAD8, ACAD8D, ACADSB |
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism. | |
Andresen BS, Christensen E, Corydon TJ, Bross P, Pilgaard B, Wanders RJ, Ruiter JP, Simonsen H, Winter V, Knudsen I, Schroeder LD, Gregersen N, Skovby F. | |
Am J Hum Genet 67(5):1095-103. Epub 2000 Sep 29. 2000 | |
3 | ACAD8 |
Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene family. | |
Telford EA, Moynihan LM, Markham AF, Lench NJ. | |
Biochim Biophys Acta 1446(3):371-6 1999 | |