threonine has been researched along with Genetic Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Choi, CR; Kim, HK; Kim, HS; Park, Q; Park, YS; Song, KS | 1 |
| Chalmers, RA; Dolphin, CT; Holmes, HC; Iles, RA; Janmohamed, A; Michelakakis, H; Murphy, HC; Phillips, IR; Shephard, EA | 1 |
2 other study(ies) available for threonine and Genetic Diseases
| Article | Year |
|---|---|
Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).
Topics: Adult; Cysteine; Female; Genetic Diseases, Inborn; Humans; Male; Pedigree; Point Mutation; Protein C; Protein C Deficiency; Recurrence; Threonine; Thrombosis | 1998 |
A novel mutation in the flavin-containing monooxygenase 3 gene, FM03, that causes fish-odour syndrome: activity of the mutant enzyme assessed by proton NMR spectroscopy.
Topics: Adult; Alleles; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Child, Preschool; Female; Genetic Diseases, Inborn; Genotype; Humans; Infant; Methylamines; Molecular Sequence Data; Mutation; Nuclear Magnetic Resonance, Biomolecular; Odorants; Oxygenases; Sequence Analysis, DNA; Syndrome; Threonine | 2000 |