proline has been researched along with Corneal Dystrophy, Juvenile Epithelial of Meesmann 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 |
|---|---|
| Baylin, EB; Clinch, TE; Daiger, SP; Font, R; Nakamura, H; Pepose, JS; Sullivan, LS; Yee, RW; Zhao, XC | 1 |
1 other study(ies) available for proline and Corneal Dystrophy, Juvenile Epithelial of Meesmann
| Article | Year |
|---|---|
A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.
Topics: Adult; Amino Acid Motifs; Arginine; Corneal Dystrophy, Juvenile Epithelial of Meesmann; Epithelium, Corneal; Exons; Genes, Dominant; Heterozygote; Humans; Keratin-12; Male; Microscopy, Electron; Molecular Biology; Mutation, Missense; Pedigree; Phenotype; Proline; Severity of Illness Index | 2007 |