norvaline has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Briand, P; Cathelineau, L | 1 |
1 other study(ies) available for norvaline and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
Sparse-fur mutation: a model for some human ornithine transcarbamylase deficiencies.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Epoxy Compounds; Hair; Immunodiffusion; Male; Mice; Mice, Mutant Strains; Mitochondria, Liver; Mutation; Ornithine; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phosphates; Valine | 1982 |