Authors:
Chakrapani, A
Olpin, S
Cleary, M
Walter, JH
Wraith, JE
Besley, GTN
Citation: A. Chakrapani et al., Trifunctional protein deficiency: Three families with significant maternalhepatic dysfunction in pregnancy not associated with E474Q mutation, J INH MET D, 23(8), 2000, pp. 826-834
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