Subject
Genetics (clinical),Genetics
Reference78 articles.
1. Aoyama T, Ushida Y, Kelley RI, et al (1993) A novel disease with deficiency of mitochondrial very long-chain acyl-CoA dehydrogenase.Biochem Biophys Res Commun 191: 1369?1372.
2. Bakker HD, Scholte HR, Jeneson JAL, Busch HFM, Abeling NGGM, van Gennip AH (1994) Vitamin-responsive complex 1 deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosis.J Inher Metab Dis 17: 196?204.
3. Beinert H (1990) Fatty acid oxidation in soluble systems of mammalian origin: the beginnings. In Tanaka K, Coates PM, eds. Fatty Acid Oxidation. Clinical, Biochemical and Molecular Aspects.Prog Clin Biol Res 321: 123?36.
4. Bennett MJ, Sherwood WG, Gibson KM, Burlina AB (1993) Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: possible metabolic markers for the primary defect.J Inher Metab Dis 16: 560?562.
5. Bennett MJ, Weinberger MJ, Sherwood WG, Burlina AB (1994) Secondary 3-hydroxydicarboxylic aciduria mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency.J Inher Metab Dis 17: 283?286.
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