leucine has been researched along with Bullous Congenital Ichthyosiform Erythroderma 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 |
|---|---|
| Endo, H; Hatamochi, A; Shinkai, H | 1 |
| Akiyama, M; Ishiko, A; Nishikawa, T; Shimizu, H; Shimizu, Y; Takizawa, Y | 1 |
2 other study(ies) available for leucine and Bullous Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
A novel mutation of a leucine residue in coil 1A of keratin 9 in epidermolytic palmoplantar keratoderma.
Topics: Amino Acid Sequence; Conserved Sequence; Female; Humans; Hyperkeratosis, Epidermolytic; Japan; Keratins; Keratoderma, Palmoplantar; Leucine; Male; Pedigree; Point Mutation; Protein Structure, Tertiary | 1997 |
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 |