proline has been researched along with Corneal Opacity in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Al Bughaili, M; Al-Gazali, L; Bahena, P; Byers, P; Callewaert, B; Choudhri, AF; Escande-Beillard, N; Fischer-Zirnsak, B; Ganesh, J; Kornak, U; Krüger, U; Lin, AE; Liu, J; Loh, A; Masri, A; Meierhofer, D; Mostafavi, R; Mundlos, S; Pajunen, L; Pivnick, EK; Rahikkala, E; Reichert, SL; Reversade, B; Robertson, SP; Robinson, PN; Sahai, I; Schwarze, U; Stolte-Dijkstra, I; Symoens, S; Tan, YX; van Ravenswaaij-Arts, C; Villarroel, CE; Wright, GD; Zemojtel, T | 1 |
| Boman, H; Bredrup, C; Knappskog, PM; Rødahl, E | 1 |
2 other study(ies) available for proline and Corneal Opacity
| Article | Year |
|---|---|
Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa.
Topics: Amino Acid Sequence; Base Sequence; Corneal Opacity; Cutis Laxa; Genes, Dominant; Humans; Intellectual Disability; Molecular Sequence Data; Mutation, Missense; Ornithine-Oxo-Acid Transaminase; Pedigree; Proline; Sequence Alignment; Sequence Analysis, DNA; Skin; Species Specificity | 2015 |
Clinical manifestation of a novel PAX6 mutation Arg128Pro.
Topics: Adult; Aged; Arginine; Cataract; Corneal Opacity; Eye Diseases, Hereditary; Eye Proteins; Female; Fovea Centralis; Homeodomain Proteins; Humans; Iris; Male; Middle Aged; Mutation, Missense; Nystagmus, Pathologic; Paired Box Transcription Factors; PAX6 Transcription Factor; Pedigree; Proline; Repressor Proteins; Retinal Diseases; Tomography, Optical Coherence | 2008 |