Authors:
Andresen, BS
Christensen, E
Corydon, TJ
Bross, P
Pilgaard, B
Wanders, RJA
Ruiter, JPN
Simonsen, H
Winter, V
Knudsen, I
Schroeder, LD
Gregersen, N
Skovby, F
Citation: Bs. Andresen et al., Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoAdehydrogenase deficiency: Identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenasesin isoleucine and valine metabolism, AM J HU GEN, 67(5), 2000, pp. 1095-1103
Authors:
Andresen, BS
Olpin, S
Kvittingen, EA
Augoustides-Savvopoulou, P
Lindhout, D
Halley, DJJ
Vianey-Saban, C
Wanders, RJA
IJlst, L
Schroeder, LD
Bolund, L
Gregersen, N
Citation: Bs. Andresen et al., DNA-based prenatal diagnosis for very-long-chain acyl-CoA dehydrogenase deficiency, J INH MET D, 22(3), 1999, pp. 281-285
Authors:
Andresen, BS
Olpin, S
Poorthuis, BJHM
Scholte, HR
Vianey-Saban, C
Wanders, R
Ijlst, L
Morris, A
Pourfarzam, M
Bartlett, K
Baumgartner, ER
deKlerk, JBC
Schroeder, LD
Corydon, TJ
Lund, H
Winter, V
Bross, P
Bolund, L
Gregersen, N
Citation: Bs. Andresen et al., Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency, AM J HU GEN, 64(2), 1999, pp. 479-494