proline has been researched along with Congenital Ichthyosiform Erythroderma 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 |
|---|---|
| Bale, SJ; Chipev, CC; Compton, JG; DiGiovanna, JJ; Korge, BP; Markova, N; Steinert, PM | 1 |
1 other study(ies) available for proline and Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis.
Topics: Amino Acid Sequence; Base Sequence; Humans; Ichthyosiform Erythroderma, Congenital; Intermediate Filaments; Keratins; Leucine; Molecular Sequence Data; Mutagenesis, Site-Directed; Proline | 1992 |