valine has been researched along with Bullous Congenital Ichthyosiform Erythroderma in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akiyama, M; Ishiko, A; Nishikawa, T; Shimizu, H; Shimizu, Y; Takizawa, Y | 1 |
1 other study(ies) available for valine and Bullous Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
A novel leucine to valine mutation in residue 7 of the helix initiation motif of keratin10 leads to bullous congenital ichthyosiform erythroderma.
Topics: Amino Acid Sequence; Child, Preschool; Humans; Hyperkeratosis, Epidermolytic; Keratins; Leucine; Male; Molecular Sequence Data; Point Mutation; Valine | 2001 |