Animal models for dicarboxylic aciduria
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF03047375
Reference20 articles.
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2. Gregersen, N. and Kolvraa, S. The occurrence of C6–C10-dicarboxylic acids, ethylmalonic acid, 5-hydroxycaproic acid, butyrylglycine, isovalerylglycine, isobutyrylglycine, 2-methylbutyrylglycine and glutaric acid in the urine of riboflavin deficient rats.J. Inker. Metab. Dis. 5, Suppl. 1 (1982) 17–18
3. Hoppel, G., DiMarco, J. P. and Tandler, B. Riboflavin and rat hepatic cell structure and function. Mitochondrial oxidative metabolism in deficiency states.J. Biol. Chem. 254 (1979) 4164–4170
4. Karpati, G., Carpenter, S., Engel, A. W., Watters, G., Allen, J., Rothman, S., Klassen, G. and Marner, O. The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical, and pathophysiological features.Neurology 25 (1975) 16–24
5. Kunau, W.-H. and Dommes, P. Degradation of unsaturated fatty acids. Identification of intermediates in the degradation ofcis-decenoyl-CoA by extracts of beef-liver mitochondria.Eur. J. Biochem. 91 (1978) 533–544
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