isoleucine has been researched along with Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans in 1 studies
| 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 | Studies |
|---|---|
| Anvret, M; Eklöf, O; Grigelioniené, G; Haereid, PE; Hagenäs, L; Neumeyer, L | 1 |
1 other study(ies) available for isoleucine and Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
| Article | Year |
|---|---|
A novel missense mutation Ile538Val in the fibroblast growth factor receptor 3 in hypochondroplasia. Mutations in brief no. 122. Online.
Topics: Achondroplasia; Amino Acid Sequence; Amino Acid Substitution; Conserved Sequence; Humans; Isoleucine; Molecular Sequence Data; Mutation, Missense; Phenotype; Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Valine | 1998 |