| 1 | ACAD8D, ACADM, ACADSB, ACADSBD, ACAT1, HSD17B10, MCCC1, MCCC2, MHBD
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| Biochemical findings in common inborn errors of metabolism.
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| Pasquali M, Monsen G, Richardson L, Alston M, Longo N.
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| Am J Med Genet C Semin Med Genet 142(2):64-76. Review. 2006
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| 2 | ACAD8, ACAD8D
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| Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans.
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| Nguyen TV, Andresen BS, Corydon TJ, Ghisla S, Abd-El Razik N, Mohsen AW, Cederbaum SD, Roe DS, Roe CR, Lench NJ, Vockley J.
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| Mol Genet Metab 77(1-2):68-79. 2002
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| 3 | ACAD8, ACAD8D, ACADSB
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| 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.
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| 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.
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| Am J Hum Genet 67(5):1095-103. Epub 2000 Sep 29. 2000
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