Page last updated: 2024-08-21

ethylmalonic acid and Ornithine Carbamoyltransferase Deficiency Disease

ethylmalonic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cyr, D; Giguère, R; Leblanc, D; Mitchell, G; Qureshi, IA	1

Other Studies

1 other study(ies) available for ethylmalonic acid and Ornithine Carbamoyltransferase Deficiency Disease

Article	Year
Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism. Biochemical and biophysical research communications, 1993, Mar-15, Volume: 191, Issue:2 Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Ammonia; Animals; Butyryl-CoA Dehydrogenase; Crosses, Genetic; Female; Genes, Recessive; Genetic Linkage; Glycine; Hair; Male; Malonates; Mice; Mice, Inbred BALB C; Mice, Mutant Strains; Mutation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Phenotype; Succinates; X Chromosome	1993

Article

Year

Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism.

Biochemical and biophysical research communications, 1993, Mar-15, Volume: 191, Issue:2

Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Ammonia; Animals; Butyryl-CoA Dehydrogenase; Crosses, Genetic; Female; Genes, Recessive; Genetic Linkage; Glycine; Hair; Male; Malonates; Mice; Mice, Inbred BALB C; Mice, Mutant Strains; Mutation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Phenotype; Succinates; X Chromosome

1993