Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: Another possible case of glutaric aciduria type II
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF02312527
Reference29 articles.
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2. Beinert, H. and Frisell, W. R. The functional identity of the electron transferring flavoproteins of the fatty acyl coenzyme A and sarcosine dehydrogenase systems.J. Biol. Chem. 237 (1962) 2988–2990
3. Björkhem, I. and Danielsson, H. Ω- and Ω-1-oxidation of fatty acids by rat liver microsomes.Eur. J. Biochem. 17 (1970) 450–459
4. Brandt, N. J., Brandt, S., Christensen, E., Gregersen, N. and Rasmussen, K. Glutaric aciduria in progressive choreoathetosis.Clin. Genet. 13 (1978) 77–80
5. Brandt, N. J., Rasmussen, K., Brandt, S., KØlvraa, S. and SchØnheyder, F.d-Glyceric acidaemia and non-ketotic hyperglycinaemia.Acta Paediatr. Scand. 65 (1976) 17–22
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