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Andresen, B. S., Christensen, E., Corydon, T. J., Bross, P., Pilgaard, B., Wanders, R. J. A., Ruiter, J. P. N., Simonsen, H., Winter, V., Knudsen, I., Schroeder, L. D., Gregersen, N., & Skovby, F. (2000). 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. American Journal of Human Genetics, 67, 1095-1103. https://doi.org/10.1086/303105
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