h 0294 has been researched along with Corneal Dystrophies 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 |
---|---|
Bateman, JB; Bhattacharya, SS; Deery, EC; Garibaldi, D; Hunt, DM; Li, Y; Lin, W; Newbold, RJ; Warren, MJ; Wilkie, SE; Zack, DJ; Zhang, H; Zhang, K | 1 |
1 other study(ies) available for h 0294 and Corneal Dystrophies
Article | Year |
---|---|
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
Topics: Amino Acid Sequence; Amino Acid Substitution; Calcium-Binding Proteins; Corneal Dystrophies, Hereditary; DNA; Female; Glutamic Acid; Glycine; Guanylate Cyclase-Activating Proteins; Humans; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Protein Conformation; Pyrimidines; Sequence Homology, Amino Acid | 2001 |