Author:
Corydon Morten Juhl,Andresen Brage Storstein,Bross Peter,Kjeldsen Margrethe,Andreasen Per Hove,Eiberg Hans,Kølvraa Steen,Gregersen Nils
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. Andresen BS, Bross P, Vianey-Saban C, Divry P, Zabot M-T, Roe CR, Nada MA, Byskov A, Kruse TA, Neve S, Kristiansen K, Knudsen I, Corydon MJ, Gregersen N (1996) Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene. Hum Mol Genet 5, 461–472 and 1390
2. Aoyama T, Souri M, Ushikubo S, Kamijo T, Yamaguchi S, Kelley RI, Rhead WJ, Uetake K, Tanaka K, Hashimoto T (1995) Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients. J Clin Invest 95, 2465–2473
3. Barton DE, Yang-Feng TL, Finocchiro G, Ozasa H, Tanaka K, Franke U (1987) Short chain acyl-CoA dehydrogenase (ACADS) maps to chromosome 12 (q22-qter) and electron transfer flavoprotein (ETFA) to 15 (q23-q25). Cytogenet Cell Genet 46, 577–578 (Abstr.)
4. Beinert H (1963) Acyl coenzyme A dehydrogenases. In The Enzymes, PD Boyer, H Lardy, K Myrback, eds. (New York: Academic Press), Vol 7, pp 447–76
5. Bhala A, Willi SM, Rinaldo P, Bennett MJ, Schmidt-Sommerfeld E, Hale DE (1995) Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency. J Pediatr 126, 910–915