Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799753
Reference41 articles.
1. Benson, E. L., Schmidt, S. Y. and Rabin, A. R. Amino acids in hereditary retinal disease. I. Plasma ornithine, lysine and taurine.Br. J. Ophthalmol. 60 (1976) 142–147
2. Berger, R. and Hommes, F. A. Regulation of pyruvate oxidation in mitochondria isolated from fetal and adult rat liver.Biochim. Biophys. Acta 314 (1973) 1–7
3. Bickel, H., Feist, D., Müller, H. and Quadbeck, G. Ornithinämie, eine weitere Aminosäurestoffwechselstörung mit Hirnschadigung.Dtsch. Med. Wochenschr. 47 (1968) 2247–2251
4. Bradford, N. M. and McGivan, J. D. Evidence for the existence of an ornithine/citrulline antiporter in rat liver mitochondria.FEBS Lett 113 (1980) 294–298
5. Brdiczka, O., Pette, D., Brunner, G. and Miller, F. Kompartmentierte Vertielung von Enzyme in Rattenlebermitochondriae.Eur. J. Biochem. 5 (1968) 294–304
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