Citations for
1ACAD8, 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
2ACAD8, 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
3ACAD8
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