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Pedersen, C. B., V. Stenbroen, R. J. A. Wanders, J. P. N. Ruiter, F. Wibrand, S. P. Young, D. S. Millington, et al. “Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Homozygosity for the common c.625G > A variation may contribute to SCAD dysfunction in cultured patient fibroblasts.” In JOURNAL OF INHERITED METABOLIC DISEASE, 31:37–37. SPRINGER, 2008.

Pedersen CB, Stenbroen V, Wanders RJA, Ruiter JPN, Wibrand F, Young SP, et al. Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Homozygosity for the common c.625G > A variation may contribute to SCAD dysfunction in cultured patient fibroblasts. In: JOURNAL OF INHERITED METABOLIC DISEASE. SPRINGER; 2008. p. 37–37.

Pedersen, C. B., et al. “Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Homozygosity for the common c.625G > A variation may contribute to SCAD dysfunction in cultured patient fibroblasts.” JOURNAL OF INHERITED METABOLIC DISEASE, vol. 31, SPRINGER, 2008, pp. 37–37.

Pedersen CB, Stenbroen V, Wanders RJA, Ruiter JPN, Wibrand F, Young SP, Millington DS, Madsen PP, Andresen BS, Moller-Larsen S, Kjeldsen M, Gregersen N. Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Homozygosity for the common c.625G > A variation may contribute to SCAD dysfunction in cultured patient fibroblasts. JOURNAL OF INHERITED METABOLIC DISEASE. SPRINGER; 2008. p. 37–37.