The frequency of MCAD mutation (K329E) in the Finnish population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/BF02029369.pdf
Reference8 articles.
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2. Similä S, Wendt L von, Ruostesuo J, Gregersen N (1984) Nonketotic C6-C10-dicarboxylic aciduria presenting as familial hepatic steatosis. (Letter) Am J Med Genet 18: 543–545
3. Matsubara Y, Kraus JP, Yang-Feng TL, Francke U, Rosenberg LE, Tanaka K (1986) Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1. Proc Natl Acad Sci 83: 6543–6547
4. Matsubara Y, Narisawa K, Miyabayashi S, Tada K, Coates PM (1990) Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiency. Lancet 335: 1589
5. Matsubara Y, Narisawa K, Tada K et al. (1991) Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase determined from Guthrie cards. Lancet 338: 552–553
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