Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, et al. (February 2008). "Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin". Molecular Genetics and Metabolism. 93 (2): 179–189. doi:10.1016/j.ymgme.2007.09.021. PMID18054510.
Corydon MJ, Andresen BS, Bross P, Kjeldsen M, Andreasen PH, Eiberg H, et al. (December 1997). "Structural organization of the human short-chain acyl-CoA dehydrogenase gene". Mammalian Genome. 8 (12): 922–926. doi:10.1007/s003359900612. PMID9383286. S2CID9157185.
Schmidt SP, Corydon TJ, Pedersen CB, Bross P, Gregersen N (June 2010). "Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress". Molecular Genetics and Metabolism. 100 (2): 155–162. doi:10.1016/j.ymgme.2010.03.009. PMID20371198.
Okuyaz C, Ezgü FS, Biberoglu G, Zeviani M, Tiranti V, Yilgör E (June 2008). "Severe infantile hypotonia with ethylmalonic aciduria: case report". Journal of Child Neurology. 23 (6): 703–705. doi:10.1177/0883073807313048. PMID18539996. S2CID46624539.
Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, et al. (August 2008). "The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level". Human Genetics. 124 (1): 43–56. doi:10.1007/s00439-008-0521-9. PMID18523805. S2CID25491212.
Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, et al. (February 2008). "Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin". Molecular Genetics and Metabolism. 93 (2): 179–189. doi:10.1016/j.ymgme.2007.09.021. PMID18054510.
Corydon MJ, Andresen BS, Bross P, Kjeldsen M, Andreasen PH, Eiberg H, et al. (December 1997). "Structural organization of the human short-chain acyl-CoA dehydrogenase gene". Mammalian Genome. 8 (12): 922–926. doi:10.1007/s003359900612. PMID9383286. S2CID9157185.
Schmidt SP, Corydon TJ, Pedersen CB, Bross P, Gregersen N (June 2010). "Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress". Molecular Genetics and Metabolism. 100 (2): 155–162. doi:10.1016/j.ymgme.2010.03.009. PMID20371198.
Okuyaz C, Ezgü FS, Biberoglu G, Zeviani M, Tiranti V, Yilgör E (June 2008). "Severe infantile hypotonia with ethylmalonic aciduria: case report". Journal of Child Neurology. 23 (6): 703–705. doi:10.1177/0883073807313048. PMID18539996. S2CID46624539.
Wolfe L, Jethva R, Oglesbee D, Vockley J (1993). "Short-Chain Acyl-CoA Dehydrogenase Deficiency". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Amemiya A (eds.). GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle. PMID21938826.
Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, et al. (August 2008). "The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level". Human Genetics. 124 (1): 43–56. doi:10.1007/s00439-008-0521-9. PMID18523805. S2CID25491212.
Corydon MJ, Andresen BS, Bross P, Kjeldsen M, Andreasen PH, Eiberg H, et al. (December 1997). "Structural organization of the human short-chain acyl-CoA dehydrogenase gene". Mammalian Genome. 8 (12): 922–926. doi:10.1007/s003359900612. PMID9383286. S2CID9157185.
Okuyaz C, Ezgü FS, Biberoglu G, Zeviani M, Tiranti V, Yilgör E (June 2008). "Severe infantile hypotonia with ethylmalonic aciduria: case report". Journal of Child Neurology. 23 (6): 703–705. doi:10.1177/0883073807313048. PMID18539996. S2CID46624539.
Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, et al. (August 2008). "The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level". Human Genetics. 124 (1): 43–56. doi:10.1007/s00439-008-0521-9. PMID18523805. S2CID25491212.