Zobrazeno 1 - 4
of 4
pro vyhledávání: '"G Daune-Anglard"'
Publikováno v:
Journal of inherited metabolic disease. 17(6)
Mice with the X-chromosomal sparse-fur (spf) mutation are an animal model of some hereditary deficiencies of ornithine carbamoyltransferase (OCT) in man. Orotic aciduria and hyperammonaemia are the most conspicuous metabolic changes in these diseases
Autor:
Seiler N; Marion Merrell Dow Research Institute, Strasbourg, France., Grauffel C, Daune-Anglard G, Sarhan S, Knödgen B
Publikováno v:
Journal of inherited metabolic disease [J Inherit Metab Dis] 1994; Vol. 17 (6), pp. 691-703.
Autor:
Seiler N; Marion Merrell Dow Research Institute, Strasbourg, France., Daune-Anglard G
Publikováno v:
Metabolic brain disease [Metab Brain Dis] 1993 Sep; Vol. 8 (3), pp. 151-79.
Autor:
Daune-Anglard G; Marion Merrell Dow Research Institute, Strasbourg, France., Bonaventure N, Seiler N
Publikováno v:
Pharmacology & toxicology [Pharmacol Toxicol] 1993 Jul; Vol. 73 (1), pp. 29-34.