Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Homozygosity for the common c.625G > A variation may contribute to SCAD dysfunction in cultured patient fibroblasts
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Pedersen, CB; Stenbroen, V; Wanders, RJA; Ruiter, JPN; Wibrand, F; Young, SP; Millington, DS; Madsen, PP; Andresen, BS; Moller-Larsen, S ...
Published in: JOURNAL OF INHERITED METABOLIC DISEASE
August 1, 2008
Duke Scholars
Published In
JOURNAL OF INHERITED METABOLIC DISEASE
ISSN
0141-8955
Publication Date
August 1, 2008
Volume
31
Start / End Page
37 / 37
Publisher
SPRINGER
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Pedersen, C. B., Stenbroen, V., Wanders, R. J. A., Ruiter, J. P. N., Wibrand, F., Young, S. P., … Gregersen, N. (2008). 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 (Vol. 31, pp. 37–37). SPRINGER.
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.
Published In
JOURNAL OF INHERITED METABOLIC DISEASE
ISSN
0141-8955
Publication Date
August 1, 2008
Volume
31
Start / End Page
37 / 37
Publisher
SPRINGER
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences